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Recalls affecting West Virginia

Data last updated: September 8, 2026 at 1:13 PM UTC

16,444 recalls found

Just announced

Straight from FDA press releases — not yet formally classified or risk-graded
UnclassifiedUndeclaredAnnounced September 4, 2026

Business Pill, Branch Manager for Mendietary supplements marketed for male sexual enhancement

Products contain undeclared yohimbine

Full report
Dietary SupplementsFood & Beverages

Recalling firm: SUPPLX.com

Grant-Valkaria, Florida - SUPPLX.com is voluntarily recalling Business Pill and Branch Manager for Men, products marketed as dietary supplements for male sexual enhancement, because FDA laboratory analysis confirmed that both products contain yohimbine that is not declared on the product labels.

Company contact: (321) 341-9501 · SupplxRecall@gmail.com

View FDA’s announcement (opens in a new tab)
UnclassifiedBacteria/virusAnnounced September 4, 2026

Foods AliveMoringa Leaf Powder

Potential to be contaminated with Salmonella

Full report
Food & BeveragesFoodborne Illness

Recalling firm: Foods Alive Inc.

Foods Alive Inc of Angola, IN, is recalling its 8-ounce packages of organic moringa leaf powder because they have the potential to be contaminated with Salmonella , an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems.

View FDA’s announcement (opens in a new tab)
UnclassifiedAnnounced September 3, 2026

B. Braun0.9% Sodium Chloride Injection USP, 100 mL, in a 150 mL PAB® Container

Presence of particulate matter identified as iron oxide

Full report
Drugs

Recalling firm: B. Braun Medical Inc.

“On September 3, 2026 firm updated their press release to include additional contaminants.” FOR IMMEDIATE RELEASE – September 3, 2026– Bethlehem, PA, B. Braun Medical Inc (B. Braun) is voluntarily recalling three (3) lots of 0.9% Sodium Chloride Injection USP, 100 mL, in a 150 mL PAB® Container, to the hospital/healthcare facility/user level due to presence of particulate matter identified as iron…

Company contact: recalls@bbraunusa.com

View FDA’s announcement (opens in a new tab)
UnclassifiedBacteria/virusAnnounced September 3, 2026

Great ValueOrganic Triple Berry Blend

Possible E. Coli Contamination

Full report
Food & BeveragesFoodborne Illness

Recalling firm: Frutas y Hortalizas del Sur S.A.

September 02, 2026. Frutas y Hortalizas del Sur S.A., San Carlos, Chile expands its July 3, 2026, recall of frozen organic IQF blueberries to include one lot of Great Value frozen Organic Triple Berry Blend 10 OZ because of potential contamination with Escherichia coli O145:H28 (E. coli O145) .

Company contact: Info.foodsafety@comfrut.com

View FDA’s announcement (opens in a new tab)
UnclassifiedAnnounced September 3, 2026

American Regent, Inc.Epinephrine Injection, USP 30 mg/ 30 mL (1 mg/mL) multi dose vial

Presence of particulate matter and lack of sterility assurance

Full report
Food & Beverages

Recalling firm: American Regent, Inc.

FOR IMMEDIATE RELEASE – September 3, 2026 – New Albany, OH, American Regent, Inc. is conducting a nationwide voluntary recall of three lots of Epinephrine Injection, USP 30 mg/ 30 mL (1 mg/mL) multi dose vials to the consumer level. Customer complaints were received for leaking and cracked vials, resulting in lack of assurance of sterility.

View FDA’s announcement (opens in a new tab)
UnclassifiedUndeclaredAnnounced August 31, 2026

LipofitLipofit Extreme 2.0 Fat Burner Dietary Supplement

Undeclared Fluoxetine and 2,4-Dinitrophenol (DNP)

Full report
Dietary SupplementsDrugs

Recalling firm: Ana Salazar Modela Tu Cuerpo Inc.

FOR IMMEDIATE RELEASE - August 27, 2026 - Davie, Florida – Ana Salazar Modela Tu Cuerpo Inc. is recalling Lipofit Extreme Fat Burner 2.0, Lot 25M12F, expiration date 09/2027, to the consumer level.

Company contact: (954) 305-1004 · yandrydy@gmail.com

View FDA’s announcement (opens in a new tab)
UnclassifiedAnnounced August 31, 2026

KofinasGarlic Mediterranean Infused Extra Virgin Olive Oil 500 ml, 250 ml, and 100 ml

Contains garlic essential oil not approved for culinary use

Full report
Food & BeveragesIngredients

Recalling firm: LMSI LLC

Cincinnati, OH (Aug. 29, 2026) - LMSI LLC/ Kofinas Olive Oil is issuing a voluntary recall of its Garlic Mediterranean infused extra virgin olive oil for using a garlic essential oil not approved for culinary use. The flavored oil was bottled in glass bottles in 500 ml, 250 ml, and 100 ml sizes.

View FDA’s announcement (opens in a new tab)
UnclassifiedAllergenUndeclaredAnnounced August 31, 2026

Little TemptationsChocolatey Eyeballs, 7 oz., 10 oz., 10.5 oz., 11 oz., and 16 oz.

Undeclared milk

Full report
Food & BeveragesAllergens

Recalling firm: Crystal Temptations

Crystal Temptations of North Arlington, NJ is recalling Halloween Chocolatey Eyeballs because they contain undeclared MILK allergens. People who have an allergy or severe sensitivity to milk run the risk of serious or life-threatening allergic reaction if they consume these products.

View FDA’s announcement (opens in a new tab)
UnclassifiedBacteria/virusAnnounced August 29, 2026

Everything SproutsRobust Radish Mix, 5oz Cups

Potential to be contaminated with Shiga toxin-producing Escherichia coli (STEC) or Salmonella.

Full report
Food & BeveragesFoodborne Illness

Recalling firm: Everything Sprouts, LLC

Everything Sprouts, LLC, based in Minneapolis, MN is expanding its voluntary recall of sprouts to include certain lots of Robust Radish Sprout Mix because it has the potential to be contaminated with Shiga toxin producing Escherichia coli (STEC) or Salmonella bacteria.

Company contact: everythingsproutsmn@gmail.com

View FDA’s announcement (opens in a new tab)
UnclassifiedBacteria/virusAnnounced August 29, 2026

MartinaMangoes

Potential contamination with Salmonella

Full report
Food & BeveragesFoodborne Illness

Recalling firm: Panorama Produce

MAMARONECK, NY, AUG. 28, 2026 - Panorama Produce is recalling 302 boxes of size 9 (nine) mangoes because they may be contaminated with Salmonella , an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems.

Company contact: information@panoramaproduce.com

View FDA’s announcement (opens in a new tab)
Wording
UnclassifiedRisk not yet known
Medical deviceRecalled August 7, 2017

Covidien Emprint Percutaneous Antenna with Thermosphere Technology, 20cm (reinforced), Material CA20L2

The firm received consumer reports of the ceramic trocar tip of the Emprint ablation antenna disengaging from the needle shaft post-ablation. This can result in the tip remaining in the patient.

ALL 50 STATES
Full report

FDA has not published a risk classification for this recall yet.

Recall #:
79075
Lot/product code:
UDI 10884521706590, Lot codes: S6MG006PX,S6MG009PX,S6MG013PX,S6MG020PX,S7AG011X,S7AG012X,S7BG008X,S7CG003X,S7DG003X,S7DG009X,S7FG001X,S7FG002X,S7FG005X,S7FG008X
Recalling firm:
Covidien LLC
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled August 7, 2017

Covidien Emprint Percutaneous Antenna with Thermosphere Technology, 30cm (reinforced), Material CA30L2

The firm received consumer reports of the ceramic trocar tip of the Emprint ablation antenna disengaging from the needle shaft post-ablation. This can result in the tip remaining in the patient.

ALL 50 STATES
Full report

FDA has not published a risk classification for this recall yet.

Recall #:
79075
Lot/product code:
UDI 10884521706606, Lot codes: S6MG007PX,S6MG010PX,S6MG016PX,S7AG002PX,S7BG005X,S7BG009X,S7DG004X,S7FG006X
Recalling firm:
Covidien LLC
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled August 7, 2017

Covidien Emprint Percutaneous Antenna with Thermosphere Technology, 15cm, Material CA15L1

The firm received consumer reports of the ceramic trocar tip of the Emprint ablation antenna disengaging from the needle shaft post-ablation. This can result in the tip remaining in the patient.

ALL 50 STATES
Full report

FDA has not published a risk classification for this recall yet.

Recall #:
79075
Lot/product code:
UDI 10884521189539, Lots S5LG002PX,S5MG004PX,S5MG009PX,S5MG010PX,S5MG013PX,S5MG017PX,S5MG019PX,S6AG002X,S6AG003X,S6AG006X,S6AG009X,S6AG010X,S6BG001X,S6BG006X,S6BG012X,S6BG013X,S6BG014PX,S6CG001X,S6CG004X,S6CG006X,S6CG007X,S6CG009X,S6CG013X,S6CG018X,S6CG019X,S6DG001X,S6DG003X,S6DG006X,S6DG008X,S6DG009X,S6EG002X,S6EG003X,S6EG005X,S6EG007X,S6EG010X,S6FG002X,S6FG003X,S6FG004X,S6FG009X,S6GG004X,S6GG005X,S6GG006X,S6GG008X,S6GG009X,S6GG011X,S6GG012X,S6GG015X,S6HG002X,S6HG010X,S6HG011X,S6HG013X,S6KG001X,S6KG004PRX,S6KG004PX,S6KG007X,S6KG008X,S6KG010X,S6KG014X,S6KG015X,S6KG017X,S6LG001X,S6LG003X,S6LG005X,S6LG006X,S6LG008X,S6LG009X,S6LG010X,S6MG001X,S6MG004X,S6MG017X,S7AG004X,S7BG002X,S7BG011PCX,S7CG009PCX,S7CG012PCX,S7CG016X,S7DG001X,S7DG006X,S7EG002X,S7EG004X,S7EG005X,S7FG009PX,S7GG001X
Recalling firm:
Covidien LLC
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled August 7, 2017

Covidien Emprint Percutaneous Antenna with Thermosphere Technology, 30cm, Material CA30L1

The firm received consumer reports of the ceramic trocar tip of the Emprint ablation antenna disengaging from the needle shaft post-ablation. This can result in the tip remaining in the patient.

ALL 50 STATES
Full report

FDA has not published a risk classification for this recall yet.

Recall #:
79075
Lot/product code:
UDI 10884521189553, Lot codes: S5LG004PX,S6AG001X,S6BG002X,S6BG005X,S6BG016PX,S6CG003X,S6CG005X,S6CG017X,S6DG004X,S6EG001X,S6FG001X,S6FG006X,S6FG010X,S6KG002X,S6KG006PRX,S6KG006PX,S6LG004X,S6MG002X,S7CG001PCX,S7CG011PCX,S7CG015CX,S7EG001X,S7EG003X,S7FG011PX
Recalling firm:
Covidien LLC
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled August 7, 2017

Covidien Emprint Percutaneous Antenna with Thermosphere Technology, 20cm, Material CA20L1

The firm received consumer reports of the ceramic trocar tip of the Emprint ablation antenna disengaging from the needle shaft post-ablation. This can result in the tip remaining in the patient.

ALL 50 STATES
Full report

FDA has not published a risk classification for this recall yet.

Recall #:
79075
Lot/product code:
UDI 10884521189546, Lot codes: S5LG003PX,S5MG016PX,S5MG018PX,S6AG004X,S6AG005X,S6AG007X,S6BG004X,S6BG011X,S6BG015PX,S6BG017X,S6CG002X,S6CG008X,S6CG014X,S6CG015X,S6CG016X,S6DG002X,S6DG005X,S6DG007X,S6DG010X,S6EG004X,S6EG006X,S6EG008X,S6FG005X,S6FG008X,S6GG007X,S6GG010X,S6HG001X,S6HG003PX,S6HG008PX,S6HG009PX,S6HG012X,S6JG001X,S6KG003X,S6KG005PRX,S6KG005PX,S6KG009X,S6KG016X,S6LG002X,S6MG003X,S6MG018X,S7AG003X,S7BG012PCX,S7CG004X,S7CG006X,S7CG008PCX,S7CG010PCX,S7CG017X,S7DG002X,S7DG005X,S7EG006X,S7FG010PX
Recalling firm:
Covidien LLC
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled August 9, 2017

Medtronic Synchromed II Model 8637 supplied in 20mL and 40 mL reservoir size and a catheter. Product Usage: The implantable Model 8637 SynchroMed II programmable pump is part of an infusion system that stores and delivers a prescribed drug to a specific site. The implanted infusion system consists of a Model 8637 SynchroMed II pump, supplied in 20 ml and 40 ml reservoir sizes, and a catheter. In the United States, the SynchroMed II Pump is specifically approved (indicated) for drugs as referenced in Indications Drug Stability and Emergency Procedures Reference Manual (refer to attached labeling # MA08927A006).

Medtronic implemented a final design change intended to address the motor stall due to corrosion and is recalling devices with the previous design that are not implanted.

ALL 50 STATES
Full report

FDA has not published a risk classification for this recall yet.

Recall #:
78609
Lot/product code:
US: CFN #: GTIN: PIN: 8637-20 00643169508149 863702012H 8637-40 00643169508156 863704012H OUS: CFN#: GTIN : PIN: 8637-20 00643169700901 863700221K 8637-20 00643169700918 863700222K 8637-20 00643169700925 863700223K 8637-20 00643169700932 863700224K 8637-20 00643169700949 863700225K 8637-20 00643169700956 863700226K 8637-20 00643169700963 863700227K 8637-20 00643169700970 863700228K 8637-20 00643169700987 863700229K 8637-20 00643169700994 863700230K 8637-20 00643169732247 863700241K 8637-20 00643169732254 863700242K 8637-20 00643169732261 863700243K 8637-20 00643169732278 863700244K 8637-20 00643169732285 863700245K 8637-20 00643169732292 863700246K 8637-20 00643169732308 863700247K 8637-20 00643169732315 863700248K 8637-20 00643169732322 863700249K 8637-20 00643169732339 863700250K 8637-40 00643169701007 863700231K 8637-40 00643169701014 863700232K 8637-40 00643169701021 863700233K 8637-40 00643169701038 863700234K 8637-40 00643169701045 863700235K 8637-40 00643169701052 863700236K 8637-40 00643169701069 863700237K 8637-40 00643169701076 863700238K 8637-40 00643169701083 863700239K 8637-40 00643169701090 863700240K 8637-40 00643169732346 863700251K 8637-40 00643169732353 863700252K 8637-40 00643169732360 863700253K 8637-40 00643169732377 863700254K 8637-40 00643169732384 863700255K 8637-40 00643169732391 863700256K 8637-40 00643169732407 863700257K 8637-40 00643169732414 863700258K 8637-40 00643169732421 863700259K 8637-40 00643169732438 863700260K
Recalling firm:
Medtronic Neuromodulation
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled August 9, 2017

Alaris Pump Module model 8100 manufactured between November 2011 and March 2012; Alaris Pump Module serviced with LVP Mechanism Sub Assembly (P/N) 10942012 between November 2011 and March 2012; Alaris Pump module Bezel Kit Assembly (P/N) 10964559) shipped between November 2011 and March 2012. The Alaris Pump module is a large volume infusion pump offered under the Alaris System. The Alaris Pump module will deliver medication and fluids using the IV administration sets for continuous or intermittent delivery through clinically acceptable routes of administration such as intravenous or epidural.

The recalling firm has received reports of increased or decreased flows that have occurred in certain pumps.

ALL 50 STATES
Full report

FDA has not published a risk classification for this recall yet.

Recall #:
77987
Lot/product code:
All Alaris Pump module model 8100 manufactured and serviced with the bezel assembly manufactured between October 2011 and November 2011; Serial Numbers - Serial 13537720 13537735 13538005 13538811 13540340 13541935 13543108 13543503 13543666 13544201 13544350 13545092 13545892 13546315 13546638 13548091 13550608 13550614 13550629 13550670 13552666 13552667 13552781 13552782 13553628 13553661 13553714 13553730 13553739 13554035 12851369 12851850 9879510 9879561 9880323 9880838 9881158 12564799 13157405 13563286 13566911 13566932 13566933 13567118 13585121 13585213 13585493 13586248 13586314 13586329 13586339 13586340 13586408 13586578 13586723 13586731 13586733 13586738 13586746 13586758 13586763 13586764 13586768 13586775 13586782 13586784 13586793 13586795 13586797 13586798 13586819 13586820 13586835 13586836 13586839 13586855 13586860 13586877 13586878 13586898 13586952 13586957 13586960 13586967 13586976 13587076 13587077 13587118 13587220 13587231 13587232 13587233 13587262 13587263 13587266 13587289 13587290 13587291 13587297 13587312 13587315 13587345 13587398 13196293 13203541 13207333 13213463 13214795 13217554 13219137 13219971 13375015 13375617 13375737 12471635 9857470 9858862 9858865 9859690 9860106 9860746 13184877 13186091 13582527 13582709 13599442 12460530 12474814 12771113 13619912 13620162 13585671 13566067 13616956 13545222 13545224 13545250 13545260 13545262 13550278 13550317 13550318 13550319 13550325 13550337 13550365 13550369 13550370 13550379 13553239 13549816 13549832 13549886 13549901 13549903 13550267 13550271 13550339 13550340 13550345 13550346 13550355 13550356 13550357 13550366 13553126 13553134 13553403 13553415 13568914 13568950 13569155 13569179 13569248 13569694 13569829 13569830 13569838 13569839 13569854 13569876 13569947 13569948 13569953 13569955 13569957 13570013 13570014 13570015 13570017 13570022 13570023 13570052 13570063 13570076 13570077 13570127 13570128 13570137 13570138 13570168 13570184 13570198 13570222 13570236 13570249 13570255 13570256 13570263 12518795 12520618 12520990 13139496 13152562 13153423 13550976 13605208 13605881 13605956 13620375 13620540 13620587 13620902 13620923 13552790 13556036 13556048 13556052 13556056 13558162 13558197 13558234 13142008 13142059 13142277 13142311 13550252 13552900 13552901 13554258 13554809 13554826 13554865 13554878 13554887 13555000 13555023 13036704 4130472 13551713 13551714 13551715 13551750 13552281 13122441 13606144 13606620 13606680 13606687 12652922 13551874 13554663 13555012 13555162 13555172 13555189 13555277 13555711 13555714 13555740 13555743 13562785 13562126 13562559 13566817 13566828 13566873 13618695 13618974 13620108 13620109 13623007 13626334 4049223 12389924 12390048 12390059 12390063 12390110 12421349 13410265 13481070 13415581 13415684 13546628 13546711 13550790 13550951 9895104 12548328 12366930 12367649 12367659 12367775 12367815 12368485 13550687 13550967 13537121 13537307 13537615 13537708 13537929 13538004 13538163 13538907 13539151 13539520 13539841 13539844 13540113 13540190 13540375 13540560 13540586 13541136 13541300 13541571 13541863 13541874 13542038 13542061 13542222 13542379 13542436 13542446 13542474 13542525 13542684 13542888 13542903 13542957 13542989 13543284 13543448 13543508 13543610 13543667 13543668 13543746 13543917 13544255 13544355 13545718 13546268 13546294 13546518 13546684 13546696 13546821 13547115 13547166 13547222 13547288 13547340 13547345 13547378 13547382 13547407 13547413 13547427 13547530 13547563 13548096 13548131 13548135 13548173 13548309 13548311 13548425 13548455 13549072 13549099 13549100 13549225 13549229 13549244 13549258 13549279 13549285 13549314 13549315 13549319 13549324 13549328 13549939 13549974 13549992 13549996 13550004 13550008 13550033 13550039 13550048 13550054 13550058 13550068 13550076 13550078 13550081 13550087 13550102 13550107 13550113 13550127 13550131 13550134 13550136 13550138 13550141 13550146 13550147 13550149 13550150 13550151 13550152 13550153 13550164 13550165 13550168 13550171 13550175 13550178 13550180 13550212 13550224 13550230 13550232 13550235 13550635 13550654 13550673 13550678 13550684 13550697 13550706 13550707 13550725 13550728 13550729 13550732 13550742 13550750 13550751 13550753 13550774 13550776 13550787 4071770 4072996 13582245 13582462 13582640 13582680 4107349 12340716 13571569 13571727 13571729 13571749 13571770 13571812 13571813 13571820 13571828 13571848 13571854 13571856 13571878 13571894 13571917 13571923 13571930 13571951 13572147 13572149 13572183 13572202 13572205 13572211 13572212 13572214 13572226 13572229 13572241 13572249 13556663 13556669 13556672 13556673 13556683 13574132 13576370 13587807 13612188 13616914 13617837 13618602 13619396 13619872 13619896 13619956 13620006 13620357 13620552 13621706 13621787 13621968 13622945 13623052 13623339 13623429 13623619 13623843 13623879 13623889 13624255 13624679 13624798 13624859 13625544 13626012 13626042 13626134 13626210 13626383 13626599 13626685 13627074 13627… (truncated, 253700 characters total — see the official FDA record for the full value)
Recalling firm:
CareFusion 303, Inc.
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled August 23, 2017

IntelliVue Multi Measurement Server, IntelliVue Multi Measurement Server SLCP, IntelliVue Multi Measurement Server X2, IntelliVue Patient Monitor Models MP2 and MP5 Product Usage: Indicated for use by health care professionals whenever there is a need for monitoring the physiological parameters of patients. Intended for monitoring, recording, and alarming of multiple physiological parameters of adults, pediatrics, and neonates in a hospital environment.

Distorted ST-Segment when using 12-Lead ECG Monitoring with Philips IntelliVue Patient Monitors

ALL 50 STATES
Full report

FDA has not published a risk classification for this recall yet.

Recall #:
78736
Lot/product code:
Model #: M300IA/AL, M3002A, M8102A, M8105A with ECO FW revision E.0 1.22 and 12-lead option C#12 Lots #s included on Consignee list  Catalog #: 862442 (M3001A), 866462 (M3001AL), 865039 (M3002A), 865040 (M8102A), 865024 (M8105A)
Recalling firm:
Philips Electronics North America Corporation
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled September 8, 2017

Sysmex Fluorocell(R) PLT Fluorocell PLT is used to stain platelets in a diluted blood sample for the counting of platelets with the Sysmex XN-Series automated hematology analyzers

There is potential that fluorescent platelet (PLT-F) and immature platelet fraction (IPF%, #) results obtained using the lots listed above may exhibit lower than actual PLT-F and IPF values. The issue may be recognized by a large discrepancy between the impedance platelet (PLT-I) result and the PLT-F result. In most cases, the falsely decreased PLT-F results display a PLT Abn Scattergram message with an asterisk beside the result or an Action Message: Difference between PLT and PLT- F. Check the results. These are indicators of unreliable data. In rare instances, platelet flags may be absent. The PLT-I results are unaffected.

ALL 50 STATES
Full report

FDA has not published a risk classification for this recall yet.

Recall #:
78134
Lot/product code:
Lot Numbers: A6051 A6052 A6053 A6054 A6055 A6056 A6057 A6058 A6059 A6060 A6061 A6062 A6063 A6064 A6065 A6066 A6067 A6068 A6069 A6070 A6071 A6072 A6073 A6074 A6075 A6076 A6077 A6078 A6079 A6080 A6081 A6082 A6083 A6084 A6085 A6086 A6087 A6088 A6089 A6090
Recalling firm:
Sysmex America, Inc.
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled September 8, 2017

Delta Cup Beater Positioner - Aligner, model # 9057.20.555 Used during implantation of the Delta Acetabular System

An internal analysis on complaints received indicated that the welding process may have been performed sub optimally in the 12 lot # involved , leading to reduced mechanical strength of the device and possible breakage during impaction when the instrument is subjected to repeated multi-axial stresses.

ALL 50 STATES
Full report

FDA has not published a risk classification for this recall yet.

Recall #:
78109
Lot/product code:
Lot # 15AG0HJ, 15AG0HQ, 15AG0UY, 15AG00P, 15AG040, 15AG08Y, 14AG243, 15AG00Q, 15AG0UZ, 15AG0V0, 15AG0HN, 16AG02J
Recalling firm:
Limacorporate S.p.A
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled September 10, 2017

Medtronic MiniMed(TM) Quick-set(TM) (MMT-394, 394T, 399, 399T, 387, 387T, 398, 398T, 397, 397T, 386, 386T, 396, 396T)

Medtronic MiniMed(TM) Infusion Sets have the potential for over-delivery of Insulin.

ALL 50 STATES
Full report

FDA has not published a risk classification for this recall yet.

Recall #:
78125
Lot/product code:
Lot Numbers: 5179671 5179672 5179675 5179676 5179678 5179680 5174468 5174471 5185640 5185642 5185643 5185645 5185647 5185648 5185650 5176067 5176070 5176073 5176074 5176079 5176082 5176085 5185660 5185663 5185666 5185669 5185672 5185673 5176224 5176050 5176052 5176054 5176056 5189836 5189838 5189839 5173751 5173752 5189378 5189379 5189380 5174455 5174457 5174459 5174461 5189358 5189359 5189362 5189364 5189366 5185736 5174481 5174483 5174485 5174487 5189386 5189388 5189390 5189392 5189394 5189395 5179685 5179686 5179687 5179688 5179689 5170715 5170823 5170825 5170827 5173463 5174300 5173470 5173471 5173472 5173473 5173474 5173475 5173476 5173477 5170133 5170134 5170135 5179710 5179711 5179712 5179713 5179714 5179715 5179716 5179717 5179718 5179719 5179720 5179721 5179722 5179723 5179724 5179725 5179726 5179727 5179728 5170153 5170154 5170155 5179690 5179691 5179692 5179693 5179694 5179695 5179696 5179697 5179698 5179699 5179700 5179701 5179702 5179703 5179704 5179705 5175939 5175940 5176014 5176015 5176016 5176017 5176018 5176019 5176020 5176021 5176022 5176023 5176024 5176025 5180499 5180500 5180501 5180502 5180503 5180504 5180505 5180506 5180507 5180508 5180509 5180510 5180511 5180512 5180513 5180514 5180515 5180516 5180517 5180518 5185600 5185601 5185602 5185603 5185604 5185605 5185606 5185607 5185608 5185609 5185610 5185611 5185612 5185613 5185614 5185615 5185616 5185617 5185618 5185619 5188097 5188098 5188099 5188100 5188101 5188102 5188103 5188104 5188105 5188106 5188107 5188108 5188109 5188110 5188111 5188112 5188113 5188114 5188115 5189846 5189847 5189852 5189853 5171629 5171630 5171631 5171632 5171633 5171634 5171635 5171636 5171637 5171638 5171639 5171640 5171641 5171642 5171643 5171644 5171645 5171646 5171647 5171648 5176026 5176027 5176028 5176029 5176030 5176031 5176032 5176033 5176034 5176035 5176036 5176037 5176038 5176039 5176040 5176041 5176042 5176043 5176044 5176045 5179790 5179791 5179792 5179793 5179794 5179795 5179796 5179797 5179798 5179799 5179800 5179801 5179802 5179803 5179804 5179805 5179806 5179807 5179808 5179809 5179810 5179811 5179812 5179813 5179814 5179815 5179816 5179817 5179818 5179819 5180479 5180480 5180481 5180485 5179758 5179759 5179760 5179761 5179762 5179763 5179764 5179765 5179766 5179767 5179768 5179769 5179770 5179771 5179772 5179773 5179774 5179775 5179776 5179777 5179778 5179779 5179780 5179781 5179782 5179783 5179784 5179785 5179786 5179787 5179788 5179789 5185620 5185621 5185622 5185623 5185624 5185625 5185626 5185627 5185628 5185629 5185630 5185631 5185632 5185633 5185634 5185635 5185636 5185637 5185638 5185639 5189406 5189407 5189408 5189409 5189410 5189411 5189412 5189413 5189414 5189415 5189416 5189417 5189418 5189419 5189420 5189421 5189422 5189423 5189424 5189425 5189426 5189427 5189428 5189429 5189430 5189431 5195705 5181716 5181718 5181720 5181722 5181723 5189446 5189449 5189451 5189452 5180519 5180522 5180525 5180528 5180530 5180531 5180533 5170898 5170901 5170904 5182140 5182143 5182145 5182146 5182149 5170619 5170622 5182158 5182161 5182163 5182164 5182166 5182167 5165412 5182139 5188235 5173794 5173795 5173796 5173797 5173798 5173799 5173800 5173801 5173802 5173803 5173804 5173805 5173806 5173807 5173808 5173809 5173810 5173811 5173812 5173813 5173814 5173815 5173816 5173817 5173818 5173819 5173820 5173821 5173822 5173823 5173824 5173825 5173826 5173827 5173828 5173829 5173830 5173831 5173832 5180451 5180452 5180453 5180454 5180455 5180456 5180457 5180458 5180459 5180460 5180461 5180462 5180463 5180464 5180465 5180466 5180467 5180468 5180469 5180470 5185480 5185481 5170855 5170856 5170857 5170858 5173753 5173754 5173755 5173756 5173757 5173758 5173759 5173760 5173761 5173762 5173763 5173764 5173765 5173766 5173767 5173768 5173769 5173770 5173771 5173772 5173773 5173774 5173775 5173776 5173777 5173778 5173779 5173780 5173781 5173782 5173783 5173784 5173785 5173786 5173787 5173788 5173789 5175967 5175968 5175969 5175970 5175971 5175972 5175973 5175974 5175975 5175976 5175977 5175978 5175979 5175980 5175981 5175982 5175983 5175984 5175985 5185590 5185591 5185592 5185593 5185594 5185595 5185596 5185597 5185598 5185599 5190564 5190565 5175947 5175948 5175950 5175951 5189466
Recalling firm:
Medtronic Inc.
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled September 10, 2017

Medtronic MiniMed(TM) Sure-T(TM) (MMT-862, 862T, 864, 864T, 866, 866T, 874, 874T, 876, 876T, 884, 886, 886T)

Medtronic MiniMed(TM) Infusion Sets have the potential for over-delivery of Insulin.

ALL 50 STATES
Full report

FDA has not published a risk classification for this recall yet.

Recall #:
78125
Lot/product code:
Lot Numbers: 5188321 5190185 5190186 5184968 5185467 5185468 5185469 5185470 5188322 5188323 5188324 5188325 5188326 5188327 5188328 5189476 5189477 5189478 5189521 5189522 5190187 5190188 5190189 5191046 5191047 5191355 5192532 5183060 5183061 5187300 5187301 5187556 5187557 5189051 5193052 5188329 5188330 5189053 5189054 5194937 5185690 5187558 5191357 5187559
Recalling firm:
Medtronic Inc.
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled September 10, 2017

Medtronic MiniMed(TM) Mio(TM) (MMT-921, 921T, 923, 923T, 925, 925T, 941, 941T, 943, 943T, 945, 945T, 961, 963, 963T, 965, 965T, 975, 975T)

Medtronic MiniMed(TM) Infusion Sets have the potential for over-delivery of Insulin.

ALL 50 STATES
Full report

FDA has not published a risk classification for this recall yet.

Recall #:
78125
Lot/product code:
Lot Numbers: 5079672 5079674 5079675 5079697 5079698 5082268 5082622 5082773 5084125 5084460 5084464 5085187 5086974 5087586 5088981 5091305 5095068 5095069 5095177 5095195 5097241 5097967 5098225 5101297 5101624 5103311 5103312 5103409 5103888 5104247 5104632 5106185 5109341 5109702 5109707 5109788 5109789 5109790 5109791 5115440 5115456 5117215 5117935 5119233 5119933 5122173 5122398 5123224 5123228 5123253 5123254 5127870 5127932 5129136 5130064 5130084 5131255 5131853 5131854 5132018 5132951 5133982 5134548 5135127 5135128 5135176 5139007 5140383 5140384 5141588 5143411 5143418 5143983 5143984 5146890 5147485 5148153 5148887 5149493 5150551 5150591 5151310 5151829 5152526 5152962 5153937 5154653 5156088 5156857 5157422 5158190 5158191 5161065 5162223 5162250 5162886 5163245 5163931 5163949 5166387 5167139 5167818 5167819 5169320 5169321 5174510 5176569 5176581 5177287 5178033 5180040 5180041 5068343 5119941 5127869 5127940 5140277 5140347 5150562 5153947 5162256 5165229 5167006 5169334 5175719 5180060 5078337 5079699 5079702 5082269 5082270 5082627 5082774 5082775 5084126 5084127 5084462 5085476 5086923 5087587 5087588 5088385 5088386 5088612 5088613 5088982 5088983 5088984 5088985 5091306 5091307 5095070 5095071 5095072 5095181 5095183 5095196 5095197 5096419 5096420 5096423 5097242 5097968 5098226 5098599 5098828 5099489 5099719 5099720 5100589 5100590 5101625 5101626 5103313 5103314 5103315 5103889 5104633 5104634 5105363 5105364 5105437 5106827 5106828 5107548 5109709 5109711 5109792 5109793 5109794 5109795 5109796 5115441 5115444 5115454 5115455 5117039 5117216 5117267 5117936 5117937 5117938 5117939 5118541 5119234 5119663 5119934 5120632 5120633 5122399 5122400 5122401 5122402 5123226 5123227 5127871 5128409 5128411 5128412 5128413 5128448 5128449 5129142 5130065 5130066 5130067 5131256 5131257 5131855 5131856 5131857 5131858 5132095 5132099 5132952 5132953 5133983 5133984 5134433 5134549 5134550 5135129 5135130 5135131 5136421 5137569 5137570 5137881 5139008 5139009 5140271 5140385 5140386 5140387 5140388 5140389 5140391 5140392 5141466 5141511 5141512 5143412 5143985 5143986 5143987 5143988 5143989 5144245 5146891 5147486 5147487 5149494 5149495 5149496 5150428 5150471 5150472 5150473 5151301 5151830 5151831 5151832 5152963 5152964 5153938 5154654 5154655 5155461 5155462 5156446 5156447 5157364 5157371 5157372 5157423 5157424 5158192 5158193 5158194 5158195 5161066 5161067 5161460 5161461 5161815 5162224 5162225 5162251 5162252 5162889 5163246 5163247 5163258 5163932 5164574 5164575 5165202 5165203 5165204 5165990 5165991 5167802 5167803 5167804 5167805 5167806 5169322 5169323 5170778 5172578 5172579 5172580 5174511 5174512 5174513 5174514 5174515 5175706 5175707 5175708 5176470 5176471 5177285 5177286 5177288 5177289 5178180 5178181 5178182 5178183 5180042 5180045 5180046 5104249 5106559 5107119 5115452 5122416 5122417 5128451 5146898 5148922 5154662 5163261 5165960 5167136 5178184 5078343 5079703 5081819 5084130 5084466 5088387 5088986 5094245 5095073 5095204 5097243 5098829 5105435 5106186 5109718 5109797 5109798 5115457 5117217 5118542 5118929 5122174 5122403 5122581 5127872 5129134 5130068 5130069 5131258 5131859 5135132 5135133 5135134 5136422 5138172 5139010 5140393 5140394 5141470 5143413 5143990 5147488 5150558 5151302 5153939 5154270 5155463 5156832 5157425 5158196 5163933 5165206 5165957 5167807 5169324 5174516 5177290 5180047 5181092 5077112 5077135 5078333 5078335 5079704 5081818 5082271 5082776 5082777 5085188 5085189 5086975 5087589 5088389 5088989 5090810 5091221 5091308 5091309 5095074 5095206 5095587 5096424 5097244 5097969 5098227 5098830 5101627 5103316 5103317 5103890 5105444 5105446 5106187 5106188 5106829 5107549 5109799 5109800 5109801 5109802 5115442 5115443 5117041 5117218 5117219 5117246 5117940 5118543 5119235 5119935 5120634 5122175 5122404 5122405 5122582 5123230 5123240 5123241 5129131 5129132 5129133 5129486 5130070 5131259 5131860 5131861 5132965 5133985 5135135 5135136 5135470 5136423 5137370 5137876 5138173 5139011 5140272 5140395 5140396 5141586 5141601 5143414 5143674 5143991 5143992 5146899 5147489 5148154 5148444 5148888 5150474 5150475 5151276 5151303 5151833 5151834 5152541 5152965 5153940 5154656 5156448 5156833 5157370 5157426 5157427 5158197 5158198 5161074 5161814 5162024 5162253 5163248 5163950 5163951 5164576 5166402 5167808 5170779 5170780 5174517 5174518 5175704 5175709 5176568 5176577 5178025 5178186 5180048 5068344 5090864 5113373 5119959 5120571 5127937 5127941 5140278 5140346 5150563 5151309 5162257 5162869 5169335 5170600 5174531 5176575 5180061 5078266 5078938 5079676 5079678 5079707 5079708 5079709 5082272 5082441 5082442 5082446 5082615 5082616 5082778 5084128 5084129 5084468 5084469 5084470 5084471 5084633 5084634 5085190 5085191 5086976 5087590 5088390 5088391 5088605 5088992 5088993 5088994 5088996 5091222 5091223 5091310 5091311 5093159 5093160 5095075 5095076 5095077 5095078 5095185 5095200 5095201 5095202 5096425 5096426 5097137 50… (truncated, 11509 characters total — see the official FDA record for the full value)
Recalling firm:
Medtronic Inc.
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled September 10, 2017

Medtronic MiniMed(TM) Pro-set(TM) (MMT-280, 281)

Medtronic MiniMed(TM) Infusion Sets have the potential for over-delivery of Insulin.

ALL 50 STATES
Full report

FDA has not published a risk classification for this recall yet.

Recall #:
78125
Lot/product code:
Lot Numbers: 6211649, 6207537
Recalling firm:
Medtronic Inc.
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled September 10, 2017

Medtronic MiniMed(TM) Silhouette(TM) (MMT-377, 377T, 378, 378T, 384, 384T, 368, 368T, 381, 381T, 382, 382T, 383, 383T)

Medtronic MiniMed(TM) Infusion Sets have the potential for over-delivery of Insulin.

ALL 50 STATES
Full report

FDA has not published a risk classification for this recall yet.

Recall #:
78125
Lot/product code:
Lot Numbers: 5179979 5182542 5185471 5187173 5188894 5189581 5191349 5192467 5178077 5189588 5181137 5181140 5184757 5184758 5186199 5186203 5188890 5191350 5193510 5186206 5179854 5179857 5179975 5181712 5182176 5182543 5183121 5185154 5185157 5186200 5186201 5186202 5187102 5187170 5188889 5188893 5190033 5190708 5190710 5191351 5192470 5192679 5194101 5168207 5189592 5175824 5176442 5179855 5179977 5181711 5181713 5182177 5182179 5182544 5183122 5183123 5184087 5185155 5185156 5187101 5187171 5187817 5188886 5188887 5188888 5188895 5189583 5189584 5189585 5189586 5190031 5190707 5190709 5192468 5192469 5192471 5192680 5192691 5192692 5193308 5194100 5178081 5185473 5186207 5187821 5189590 5191354 5178084 5183072 5185153 5187103 5187818 5187819 5187820 5188892 5193505 5178076 5189591 5175953 5181138 5185472 5187172 5191352 5192682 5186205 5181139 5186204 5189587
Recalling firm:
Medtronic Inc.
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled September 20, 2017

Custom Dialysis Kit CF-4230 Without Gel, which includes Flex-Neck Classic Peritoneal Dialysis Catheter 2 Cuffs Infant Coiled, Catalog # K14-00078

1 Cuff catheters were incorrectly configured and labeled as 2 Cuff product and placed into these dialysis kits.

ALL 50 STATES
Full report

FDA has not published a risk classification for this recall yet.

Recall #:
79426
Lot/product code:
Lot #: H1190932, Exp 7/31/2020, UDI (01)00884450328613(17)200731(10)H1190932
Recalling firm:
Merit Medical Systems, Inc.
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled September 20, 2017

Flex-Neck Classic Peritoneal Dialysis Catheter 1 Cuff Infant Coiled, Catalog # CF-4235/B

2 Cuff catheters were incorrectly configured and labeled as 1 Cuff product.

ALL 50 STATES
Full report

FDA has not published a risk classification for this recall yet.

Recall #:
79426
Lot/product code:
Lot #: a) H1136644, Exp 12/31/2018, UDI (01)00884450305850(17)181231(10)H1136644; b) H1139640, Exp 12/31/18, UDI (01)00884450305850(17)181231(10)H1139640
Recalling firm:
Merit Medical Systems, Inc.
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled September 20, 2017

Custom Dialysis Kit CF-4235 Without Gel, which includes Flex-Neck Classic Peritoneal Dialysis Catheter 1 Cuff Infant Coiled, Catalog # K14-00079

2 Cuff catheters were incorrectly configured and labeled as 1 Cuff product and placed into these dialysis kits.

ALL 50 STATES
Full report

FDA has not published a risk classification for this recall yet.

Recall #:
79426
Lot/product code:
Lot #: a) H1190448, Exp 7/31/2020, UDI (01)00884450328620(17)200731(10)H1190448; b) H1193585, Exp 5/30/2019, UDI (01)00884450328620(17)190530(10)H1193585
Recalling firm:
Merit Medical Systems, Inc.
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled September 22, 2017

Prevent G Safety Winged Blood Collection Set Glide - Rx Only -Sterile/EO - Product Usage: The IMPROSAFE Blood Collection Set is single-use, sterile, winged needle bonded to a flexible tubing with luer adapter. The needle consists of (1) a winged needle, (2) a flexible tubing, (3) a luer adaptor. (4) a safety shield, The products and evacuated blood collection tube/ syringe are used together for the collection of venous blood.

Complain due to the hub needle came out when the nurse draw the blood and removed the tube.

ALL 50 STATES
Full report

FDA has not published a risk classification for this recall yet.

Recall #:
80547
Lot/product code:
Serial # 102030178 / Lot # 160815
Recalling firm:
Guangzhou Improve Medical Instruments Co., Ltd.
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled September 29, 2017

ARCHITECT c4000 part number 02P24; ARCHITECT c8000 part number 01G06; ARCHITECT c16000 part number 03L77 Clinical Chemistry systems.

The Peristaltic Head tubing placed on the ARCHITECT c4000, c8000, and c16000 has the possibility to leak due to a manufacturing issue associated with the tubing connector.

ALL 50 STATES
Full report

FDA has not published a risk classification for this recall yet.

Recall #:
78225
Lot/product code:
c400073, c400103, c400498, c400600, c400890, c400934, c400935, c401018, c401055, c401056, c401182, c401505, c401520, c401686, c401887, c460196, c460200, c460943, c461550, c803669, c803753, c1600144, c1600249, c1600251, c1600641, c1600720, c1600819, c1600859, c1600976, c1601350, c1601351
Recalling firm:
Abbott Laboratories, Inc
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled September 29, 2017

Tubing, Peristaltic Head Part Number 7-35009685-01 for use in clinical chemistry systems.

The Peristaltic Head tubing placed on the ARCHITECT c4000, c8000, and c16000 has the possibility to leak due to a manufacturing issue associated with the tubing connector.

ALL 50 STATES
Full report

FDA has not published a risk classification for this recall yet.

Recall #:
78225
Lot/product code:
Serial numbers - 125589-1-2, 125589-1-4
Recalling firm:
Abbott Laboratories, Inc
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled October 11, 2017

Carestation 620 A1, Carestation 650 A1, and Carestation 650c A1

Possible incomplete seal between the CO2 absorber and the breathing circuit CO2 bypass port assembly of the Carestation 600 Series systems.

Full report

FDA has not published a risk classification for this recall yet.

Recall #:
78469
Lot/product code:
Model No. 1012-9620-000, 1012-9650-000, 1012-9655-000, 1012-9650-002, 1012-9620-002, 1012-9655-002;   Serial Numbers: SM617100166MA SM617100163MA SM617100164MA SM617100165MA SM617100167MA SM617100168MA SM616460036MA SM616460037MA SM717200075MA SM717200072MA SM717200073MA SM717200074MA SM617300054MA SM716390006MA SM716390007MA SM716390008MA SM717020018MA SM717020019MA SM717020020MA SM717020021MA SM717020022MA SM717020023MA SM717020024MA SM717020025MA SM717200052MA SM716300041MA SM716300040MA SM716300031MA SM716480059MA SM716480060MA SM716510010MA SM716510011MA SM716510012MA SM716510013MA SM716510014MA SM616400001MA SM716380022MA SM716380023MA SM716380024MA SM616250007MA SM616460048MA SM616460049MA SM617240035MA SM617240034MA SM617170052MA SM716480021MA SM716480022MA SM716480023MA SM716480024MA SM716480025MA SM716480026MA SM716480027MA SM716480028MA SM616460022MA SM717020026MA SM717020027MA SM717020028MA SM717020029MA SM717020030MA SM616250005MA SM616400004MA SM616400005MA SM617110011MA SM617110012MA SM617110013MA SM617110014MA SM717200055MA SM717320026MA SM617310035MA SM617310032MA SM617310033MA SM617310034MA SM716510015MA SM716510016MA SM716510017MA SM717020040MA SM716300024MA SM716300025MA SM716300026MA SM716430052MA SM716430053MA SM716430054MA SM716430055MA SM717150063MA SM716480057MA SM616250001MA SM616250002MA SM616250003MA SM616250004MA SM617240031MA SM617240030MA SM717200058MA SM617340015MA SM617340013MA SM617340014MA SM617180039MA SM617180038MA SM617180042MA SM617180041MA SM617310038MA SM716480029MA SM716480030MA SM716480031MA SM716480032MA SM716480033MA SM616200020MA SM617310037MA SM617310036MA SM617310040MA SM617310039MA SM717150034MA SM717150033MA SM717150035MA SM717150036MA SM717150037MA SM717150038MA SM717150039MA SM717150047MA SM717150040MA SM717150041MA SM717150042MA SM717150043MA SM717150046MA SM717150044MA SM717150045MA SM717150048MA SM717150049MA SM717150050MA SM717150051MA SM717150052MA SM717150053MA SM717150054MA SM717150055MA SM616200019MA SM616200021MA SM616200022MA SM616200023MA SM616200024MA SM716270006MA SM716270007MA SM617010108MA SM616340023MA SM717010115MA SM717010117MA SM717010118MA SM717010120MA SM717010121MA SM717010122MA SM717010123MA SM717010124MA SM717010125MA SM717010126MA SM717010127MA SM717010128MA SM717010129MA SM717010130MA SM717010131MA SM717010132MA SM717010133MA SM717010134MA SM717010135MA SM717010136MA SM717010137MA SM717010138MA SM717010139MA SM717010140MA SM717020039MA SM717100035MA SM617180095MA SM616270021MA SM616270022MA SM717100043MA SM717100044MA SM717100045MA SM617020019MA SM617020020MA SM617020021MA SM717010116MA SM717010119MA SM616430024MA SM616460047MA SM716300027MA SM717320014MA SM717320012MA SM717320013MA SM716480058MA SM717100047MA SM717100048MA SM717100049MA SM716480055MA SM717100042MA SM716200046MA SM716200047MA SM616340001MA SM616340002MA SM616340039MA SM717010109MA SM717200051MA SM717200048MA SM717200049MA SM717200050MA SM716310001MA SM616340025MA SM616460052MA SM616460053MA SM616460054MA SM616460055MA SM616460056MA SM616460057MA SM716430066MA SM716430067MA SM716430068MA SM717200029MA SM717200026MA SM717200027MA SM717200028MA SM717200030MA SM617180102MA SM616250006MA SM717320009MA SM717320006MA SM717320007MA SM717320008MA SM717320010MA SM717320011MA SM717200098MA SM616460035MA SM617010114MA SM617010115MA SM617010116MA SM617010117MA SM617010118MA SM817080012MA SM717200047MA SM616340027MA SM616410061MA SM616340018MA SM616340019MA SM616340020MA SM717200078MA SM616460030MA SM716390011MA SM716390012MA SM616460028MA SM616460029MA SM716270001MA SM617360027MA SM617360028MA SM717320044MA SM717320045MA SM717350023MA SM616410043MA SM717020047MA SM717020048MA SM717320027MA SM717150062MA SM717150061MA SM717010104MA SM716270008MA SM617020010MA SM617020011MA SM617020012MA SM617020013MA SM617020014MA SM617020015MA SM617020016MA SM617020017MA SM617020018MA SM617140018MA SM617140015MA SM617140016MA SM617140017MA SM617260039MA SM617260038MA SM717200020MA SM617060084MA SM716250022MA SM716250023MA SM716430063MA SM716430064MA SM716430065MA SM617100056MA SM617100057MA SM616400016MA SM616400017MA SM717200085MA SM616170021MA SM616170022MA SM716300032MA SM716300033MA SM716300034MA SM716300035MA SM716300036MA SM716300037MA SM716300038MA SM716430047MA SM616200012MA SM617140033MA SM717100039MA SM717100040MA SM616340028MA SM616340029MA SM616340030MA SM716200048MA SM716200049MA SM716200050MA SM716250016MA SM716250017MA SM716250018MA SM717100056MA SM717200024MA SM717100041MA SM717100057MA SM716480056MA SM717020036MA SM716380017MA SM717200088MA SM717200086MA SM717200087MA SM717020057MA SM716380015MA SM717080055MA SM716480045MA SM716480046MA SM716480047MA SM716480048MA SM716480049MA SM716480050MA SM617100058MA SM716430050MA SM716430051MA SM716460006MA SM716460007MA SM617310008MA SM617310007MA SM617260040MA SM617260041MA SM617260042MA SM617260043MA SM617260044MA SM716300044MA SM716300045MA SM616340021MA SM716460023MA SM716460024MA SM716460025MA SM716460026MA SM716460027MA SM7164600… (truncated, 253347 characters total — see the official FDA record for the full value)
Recalling firm:
GE Medical Systems China Co., Ltd.
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled October 11, 2017

Carestation 620 A2, Carestation 650 A2, and Carestation 650c A2

Possible incomplete seal between the CO2 absorber and the breathing circuit CO2 bypass port assembly of the Carestation 600 Series systems.

Full report

FDA has not published a risk classification for this recall yet.

Recall #:
78469
Lot/product code:
Model No. 1012-9620-000, 1012-9650-000, 1012-9655-000, 1012-9650-002, 1012-9620-002, 1012-9655-002;   Serial No. SM617240023WA-A2, SM617240022WA-A2 SM617250011WA-A2 SM617240010WA-A2 SM617240011WA-A2 SM617240003WA-A2 SM617240012WA-A2 SM617240004WA-A2 SM717180002WA-A2 SM717250002WA-A2 SM717230002WA-A2 SM717250003WA-A2 SM717250011WA-A2 SM717250010WA-A2 SM817240005WA SM817240003WA SM817240004WA SM617230006WA SM617230066WA SM617230067WA SM617230068WA SM617230069WA SM617230070WA SM617230071WA SM617230072WA SM617230073WA SM617230074WA SM617230075WA SM617230076WA SM617230077WA SM617230079WA SM617230078WA SM617250041WA SM617250040WA SM617230081WA SM617230080WA SM617240009WA SM617240019WA SM617240016WA SM617240017WA SM617240018WA SM617240024WA SM617250012WA SM617250009WA SM617250005WA SM617250003WA SM617250019WA SM617250004WA SM617250010WA SM617250023WA SM617250022WA SM617250024WA SM617250028WA SM617250025WA SM617250026WA SM617250027WA SM617250029WA SM617250030WA SM617250031WA SM617250032WA SM617250033WA SM617250034WA SM617250038WA SM617250035WA SM617250039WA SM617250036WA SM617250037WA SM617320008WA SM617330010WA SM617330009WA SM617370027WA SM617230003WA SM617230002WA SM617250016WA SM617250013WA SM617250014WA SM617250015WA SM617250017WA SM617250020WA SM617250002WA SM617250001WA SM617360038WA SM617380014WA SM617250018WA SM617370028WA SM617240008WA SM617240005WA SM617240006WA SM617240007WA SM617280005WA SM617330008WA SM617330006WA SM617330007WA SM617370016WA SM617370087WA SM617370084WA SM617370085WA SM617370086WA SM617370088WA SM617370018WA SM617370017WA SM617370015WA SM617370008WA SM617250021WA SM617280015WA SM617280014WA SM617280016WA SM617280018WA SM617280022WA SM617280019WA SM617280020WA SM617280021WA SM617280023WA SM617280024WA SM617280025WA SM617280026WA SM617280027WA SM617280028WA SM617280029WA SM617280030WA SM617280031WA SM617280032WA SM617280033WA SM617290005WA SM617290006WA SM617290007WA SM617290008WA SM617280017WA SM617330023WA SM617370006WA SM617370004WA SM617370005WA SM617360037WA SM617380004WA SM617380001WA SM617380002WA SM617380003WA SM617380005WA SM617380006WA SM617380007WA SM617380008WA SM617380009WA SM617360004WA SM617370007WA SM617370022WA SM617370019WA SM617370020WA SM617370021WA SM617370023WA SM617370024WA SM617370003WA SM617370001WA SM617370002WA SM617370012WA SM617370009WA SM617370010WA SM617370011WA SM617370013WA SM617370014WA SM617360040WA SM617380013WA SM717250005WA SM717250007WA SM717320001WA SM717230003WA SM717230005WA SM717230004WA SM717260002WA SM717260001WA SM717370004WA SM717370003WA SM717250006WA SM717370001WA SM717250016WA SM717250014WA SM717250015WA SM717250013WA SM717330008WA SM717370002WA SM717370018WA SM817210001WA SM817210002WA SM717330016WA;   UDI No.: 010084068210398521SM617250012WA11170624, 010084068210398521SM617250003WA11170619, 010084068210398521SM617250004WA11170619, 010084068210398521SM617250010WA11170621, 010084068210398521SM617250013WA11170624, 010084068210394721SM717260002WA11170627, 010084068210394721SM717260001WA11170627, 010084068210395421SM817210001WA11170522, 010084068210395421SM817210002WA11170522
Recalling firm:
GE Medical Systems China Co., Ltd.
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled October 16, 2017

Fukuda Denshi patient monitor model DS-8100M and DS-8100N Product Usage: Use of the Fukuda Denshi DynaScope Model DS-8100N/8100M Patient Monitor is indicated in those situations where observation of one or more of the following parameters on an individual patient may be required. ECG (waveform, heart rate, ST-Level and ventricular arrhythmias), respiration, non-invasive blood pressure (NIBP), pulse rate, arterial oxygen saturation (SpO2), carboxyhemoglobin saturation (SpCO)*, methemoglobin saturation (SpMet)*, total hemoglobin concentration (SpHb)*, plethysmograph, temperature, invasive blood pressure (IBP), cardiac output, and carbon dioxide concentration (CO2). *: DS-8100M only The target populations of the system are adult, pediatric and neonatal patients with the exception of the ST segment, arrhythmia analysis, and SpHb, for which the target populations are adult and pediatric excluding neonates. These observations can include an audible and visual alarm if any of these parameters exceed values that are established by the clinician. The observations may include the individual or comparative trending of one or more of these parameters over a period of up to 24 hours. The DS-8100N/8100M Patient Monitor is indicated in situations where an instantaneous display of waveform, numeric and trended values is desired. The DS-8100N/8100M Patient Monitor is also indicated where a hard copy record of the physiological parameters, the alarms conditions or the trended values may be required.

For the Fukuda Denshi patient monitor model DS-8100, in less than 0.003% (17) of the 6227 devices sold worldwide, a Short-term Battery Error message has appeared and has been traced back to a bad (damaged) Lithium-Ion capacitor (Short-term battery backup).

ALL 50 STATES
Full report

FDA has not published a risk classification for this recall yet.

Recall #:
78441
Lot/product code:
all DS-8100 units manufactured and distributed worldwide.
Recalling firm:
Fukuda Denshi Co., Ltd.
View official FDA record (opens in a new tab)
Class IIModerate risk
FoodUndeclaredRecalled October 19, 2017

bliss anti-stress formula Dietary Supplement, 60 Tablets; Manufactured For and distributed by: Market America, Inc., 1302 Pleasant Ridge Road, Greensboro, NC 27409; UPC 8 48570 00470 3

Potentially not listed on the label Yohimbe 83 and complaints of adverse reactions: upset stomach, jittery, sweaty, lightheaded or dizzy.

Full report

A moderate-risk recall. Using this product might cause temporary or reversible health problems, and serious harm is unlikely.

Recall #:
F-0681-2020
Lot/product code:
Lot #: 51130, Expiration Date: 07/2019 Manufacturer's Code PK-MA13173 Manufacturer's Item #Z02320
Recalling firm:
Market America Inc
View official FDA record (opens in a new tab)