BIGNOPE
Ko-fi

Recalls affecting Wyoming

Data last updated: September 10, 2026 at 1:16 PM UTC

16,268 recalls found
NewOld
High RiskLow Risk
AllClear

Just announced

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

Business Pill, Branch Manager for Men — dietary 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/virusSalmonellaAnnounced September 4, 2026

Foods Alive — Moringa 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. Braun — 0.9% 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/virusE. coliAnnounced September 3, 2026

Great Value — Organic 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)
UnclassifiedAllergenMilkUndeclaredAnnounced August 31, 2026

Little Temptations — Chocolatey 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)
UnclassifiedUndeclaredAnnounced August 31, 2026

Lipofit — Lipofit 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

Kofinas — Garlic 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)
UnclassifiedBacteria/virusSalmonellaE. coliAnnounced August 29, 2026

Everything Sprouts — Robust 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/virusSalmonellaAnnounced August 29, 2026

Martina — Mangoes

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 May 1, 2021

Continuous CT Fluoroscopy DVI Ceiling Mount CCT Arm DVI Option - Monitor Bracket Assembly for use with CT and PET/CT systems. Brilliance 16 Power, Brilliance 16/10/6 Water/Air 728240/728245/728246 - Brilliance 16 728255/728256/728266 - Brilliance 6 728250/728251 - Brilliance 10 728260 - Extended Brilliance Workspace

Significant wear of the Monitor Bracket Assembly shaft goes unrecognized could potentially lead to the Monitor Bracket Assembly detaching from the Suspension Arm and result in potential hazard for the monitor to fall while remaining attached to the cables resulting in patient, operator, bystander, or service person to serious injury.

ALL 50 STATES
▸Full report

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

Recall #:
87974
Lot/product code:
Model/ Serial Number/UDI: N/A 728240 60005 728240 60003 728240 6017 728240 60012 728240 60007 728240 6105 728240 6136 728240 60016 728240 60014 728240 60006 728240 6156 728240 5080 728240 60011 728240 6109 728240 5413  728245 3371 728245 3394 728245 3484_ 728245 3500 728245 3377 728245 . 728245 3448 728245 3483 728245 3443 728245 3360 728245 9732 728245 3426 728245 3429 728245 6109 728245 3408 728245 3473 728245 3419  728246 260032 728246 6444 728246 6265 728246 5452 728246 40018 728246 6618 728246 50081 728246 50014 728246 50026 728246 6556 728246 5449 728246 50029 728246 5485 728246 5942 728246 50046 728246 30019 728246 5313 728246 5013 728246 50096 728246 5207 728246 5916 728246 50094 728246 30033 728246 50032 728246 5174 728246 6503 728246 6519 728246 6511 728246 5773 728246 5816 728246 260015 728246 6491 728246 5296 728246 50188 728246 30103 728246 5041 728246 4017 728246 5632 728246 50010 728246 5658 728246 3382 728246 30063 728246 5515 728246 5343 728246 50053 728246 5621 728246 6141 728246 50209 728246 5431 728246 9374 728246 50005 728246 6632 728246 50025 728246 30109 728246 5754 728246 50211 728246 5078 728246 3170 728246 6255 728246 3014 728246 5097 728246 6612 728246 5812 728246 60013 728246 6533 728246 50134  728255 9802 728255 9728 728255 9795  728256 3382 728256 30103 728256 30100 728256 3014 728256 3296 728256 3463 728256 3344 728256 30029 728256 3113 728256 3063 728256 30110 728256 30063  728266 3635  728250 2579  728251 40008 728251 40004 728251 40006 728251 4005 728251 3008 728251 40021 728251 40019  728260 7330 N/A 728260 12323 N/A
Recalling firm:
Philips North America Llc
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled May 1, 2021

Continuous CT Fluoroscopy DVI Ceiling Mount CCT Arm DVI Option - Monitor 728306 - Brilliance iCT 728311 - Brilliance iCT SP

Significant wear of the Monitor Bracket Assembly shaft goes unrecognized could potentially lead to the Monitor Bracket Assembly detaching from the Suspension Arm and result in potential hazard for the monitor to fall while remaining attached to the cables resulting in patient, operator, bystander, or service person to serious injury.

ALL 50 STATES
▸Full report

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

Recall #:
87974
Lot/product code:
Model/ Serial Number/UDI: N/A System Code System Serial Number Unique Device Identifier (UDI#) 728306 100788 N/A 728306 100857 (01)00884838059474(21)100857 728306 100739 N/A 728306 100394 N/A 728306 100625 N/A 728306 100664 N/A 728306 100764 (01)00884838059474(21)100764 728306 100280 N/A 728306 100782 (01)00884838059474(21)100782 728306 100830 (01)00884838059474(21)100830 728306 100410 N/A 728306 100413 N/A 728306 100788 N/A 728306 100322 N/A 728306 100374 N/A 728306 100327 N/A 728306 100463 N/A 728306 85033 N/A 728306 85104 N/A 728306 85125 (01)00884838059474(21)85125 728306 85095 (01)00884838059474(21)85095 728306 85018 N/A 728306 85013 N/A 728306 100400 N/A 728306 100402 N/A 728306 100405 N/A 728306 100509 N/A 728306 100331 N/A 728306 100375 N/A 728306 100056 N/A 728306 85019 N/A 728306 100657 N/A 728306 100415 N/A 728306 100507 N/A 728306 100450 N/A 728306 100386 N/A 728306 85113 (01)00884838059474(21)85113 728306 100281 N/A 728306 100441 N/A 728306 100346 N/A 728306 100300 N/A 728306 85039 N/A 728306 100348 N/A 728306 100347 N/A 728306 100345 N/A 728306 100490 N/A 728306 100667 N/A 728306 85054 N/A 728306 100335 N/A 728306 100404 N/A 728306 100604 N/A 728306 100408 N/A 728306 100317 N/A 728306 342002 N/A 728306 85219 (01)00884838059474(21)85219 728306 100682 N/A 728306 100313 N/A 728306 100332 N/A 728306 100092 N/A 728306 100163 N/A 728306 100646 N/A 728306 100714 N/A 728306 85031 N/A 728306 100411 N/A 728306 100720 N/A 728306 100610 N/A 728306 100653 N/A 728306 100517 N/A 728306 85101 (01)00884838059474(21)85101 728306 100632 N/A 728306 100062 N/A 728306 100288 N/A 728306 100365 N/A 728306 100169 N/A 728306 100858 (01)00884838059474(21)100858 728306 100446 N/A 728306 100813 (01)00884838059474(21)100813 728306 100729 N/A 728306 100601 N/A 728306 100205 N/A 728306 100038 N/A 728306 100302 N/A 728306 100723 N/A 728306 N/A 728306 100086 (01)00884838059474(21)100086 728306 100791 (01)00884838059474(21)100791 728306 100193 N/A 728306 85218 (01)00884838059474(21)85218 728306 100638 N/A 728306 100440 N/A 728306 100223 N/A 728306 100645 N/A 728306 100414 N/A 728306 100260 N/A 728306 100314 N/A 728306 100339 N/A 728306 85012 N/A 728306 100299 N/A 728306 100115 N/A 728306 100278 N/A 728306 85097 (01)00884838059474(21)85097 728306 100357 N/A 728306 100412 N/A 728306 100409 N/A 728306 100794 (01)00884838059474(21)100794 728306 100123 N/A 728306 100622 N/A 728306 100631 N/A 728306 100349 N/A 728306 100147 N/A 728306 85029 N/A 728306 100681 N/A 728306 87008 (01)00884838059474(21)87008 728306 85221 (01)00884838059474(21)85221 728306 100144 N/A 728306 85038 N/A 728306 100372 N/A 728306 100044 N/A 728306 100623 N/A 728306 85078 N/A 728306 85202 (01)00884838059474(21)85202 728306 85205 (01)00884838059474(21)85205 728306 100341 N/A 728306 100503 N/A 728306 100325 N/A 728306 100290 N/A 728306 100406 N/A 728306 85127 (01)00884838059474(21)85127 728306 100634 N/A 728306 100064 N/A 728306 100759 (01)00884838059474(21)100759 728306 100040 N/A 728306 100679 N/A 728306 100654 N/A 728306 100416 N/A 728306 100396 N/A 728306 85276 (01)00884838059474(21)85276 728306 100257 N/A 728306 100466 N/A 728306 100453 N/A 728306 100452 N/A 728306 85230 N/A 728306 100351 N/A 728306 85138 (01)00884838059474(21)85138 728306 85285 (01)00884838059474(21)85285 728306 100689 N/A 728306 100626 N/A 728306 100454 N/A 728306 100486 N/A 728306 100633 N/A 728306 87047 (01)00884838059474(21)87047 728306 85283 (01)00884838059474(21)85283 728306 N/A N/A 728306 85145 (01)00884838059474(21)85145 728306 100821 (01)00884838059474(21)100821 728306 100368 N/A 728306 85080 (01)00884838059474(21)85080 728306 100804 (01)00884838059474(21)100804 728306 100802 (01)00884838059474(21)100802 728306 87036 (01)00884838059474(21)87036 728306 100806 (01)00884838059474(21)100806 728306 100501 N/A 728306 100373 N/A 728306 100853 (01)00884838059474(21)100853 728306 100661 N/A 728306 100381 N/A 728306 100852 (01)00884838059474(21)100852 728306 100287 N/A 728306 100045 N/A 728306 85099 (01)00884838059474(21)85099 728306 100462 N/A 728306 85286 (01)00884838059474(21)85286  728311 200119 N/A 728311 83006 (01)00884838059481(21)83006 728311 83009 N/A 728311 200090 N/A 728311 200039 N/A 728311 200137 N/A 728311 200052 N/A 728311 200058 N/A 728311 200078 N/A 728311 83005 (01)00884838059481(21)83005 728311 200011 N/A 728311 200006 N/A 728311 200022 N/A 728311 200018 N/A 728311 200214 N/A 728311 200093 N/A 728311 200101 N/A 728311 200107 N/A 728311 200138 N/A 728311 200121 N/A 728311 200021 (01)00884838059474(21)200021 728311 200213 N/A 728311 200068 N/A 728311 200127 N/A 728311 83002 (01)00884838059481(21)83002 728311 200047 N/A 728311 644 N/A 728311 200089 N/A 728311 200082 N/A 728311 200112 N/A 728311 200217 (01)00884838059481(21)200217 728311 200205 N/A 728311 200203 N/A
Recalling firm:
Philips North America Llc
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled May 1, 2021

Continuous CT Fluoroscopy DVI Ceiling Mount CCT Arm DVI Option - Monitor 728333 - Spectral CT:

Significant wear of the Monitor Bracket Assembly shaft goes unrecognized could potentially lead to the Monitor Bracket Assembly detaching from the Suspension Arm and result in potential hazard for the monitor to fall while remaining attached to the cables resulting in patient, operator, bystander, or service person to serious injury.

ALL 50 STATES
▸Full report

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

Recall #:
87974
Lot/product code:
Model/ Serial Number/UDI: N/A 10016 (01)00884838101111(21)10016 10018 (01)00884838101111(21)10018
Recalling firm:
Philips North America Llc
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled May 1, 2021

Continuous CT Fluoroscopy DVI Ceiling Mount - CCT Arm DVI Option - Gemini GXL 16 Slice System Number: 882410 Continuous CT (CCT) is a CT or PET/CT product option that enables physicians and radiologists to produce real-time CT images to facilitate image-guided surgery.

Significant wear of the Monitor Bracket Assembly shaft may go unrecognized could lead to the Monitor Bracket Assembly detaching from the Suspension Arm, and resulting in injury to patient, operator, bystander, or service person located in the path of a falling part

ALL 50 STATES
▸Full report

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

Recall #:
89039
Lot/product code:
Serial Number: 4165
Recalling firm:
Philips North America Llc
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled May 1, 2021

Continuous CT Fluoroscopy DVI Ceiling Mount - CCT Arm DVI Option - Gemini TF 64 System Number: 882471 Continuous CT (CCT) is a CT or PET/CT product option that enables physicians and radiologists to produce real-time CT images to facilitate image-guided surgery.

Significant wear of the Monitor Bracket Assembly shaft may go unrecognized could lead to the Monitor Bracket Assembly detaching from the Suspension Arm, and resulting in injury to patient, operator, bystander, or service person located in the path of a falling part

ALL 50 STATES
▸Full report

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

Recall #:
89039
Lot/product code:
Serial Number: 7141 7218 7229 7245
Recalling firm:
Philips North America Llc
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled May 1, 2021

Continuous CT Fluoroscopy DVI Ceiling Mount - CCT Arm DVI Option - Gemini TF 16 System Number: 882470 Continuous CT (CCT) is a CT or PET/CT product option that enables physicians and radiologists to produce real-time CT images to facilitate image-guided surgery.

Significant wear of the Monitor Bracket Assembly shaft may go unrecognized could lead to the Monitor Bracket Assembly detaching from the Suspension Arm, and resulting in injury to patient, operator, bystander, or service person located in the path of a falling part

ALL 50 STATES
▸Full report

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

Recall #:
89039
Lot/product code:
Serial Number: 7084 7145 7584
Recalling firm:
Philips North America Llc
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled May 1, 2021

Continuous CT Fluoroscopy DVI Ceiling Mount - CCT Arm DVI Option - TruFlight Select PET/CT System Number: 882438 Continuous CT (CCT) is a CT or PET/CT product option that enables physicians and radiologists to produce real-time CT images to facilitate image-guided surgery.

Significant wear of the Monitor Bracket Assembly shaft may go unrecognized could lead to the Monitor Bracket Assembly detaching from the Suspension Arm, and resulting in injury to patient, operator, bystander, or service person located in the path of a falling part

ALL 50 STATES
▸Full report

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

Recall #:
89039
Lot/product code:
Serial Number: 17006
Recalling firm:
Philips North America Llc
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled May 4, 2021

Atellica CH 930 Analyzer with Photometer Lamp (SMN 11075676) Siemens Material Number: 11067000

Photometer Lamp May Reach Saturation Without Flagging Results, may generate erroneously elevated or depressed patient results

ALL 50 STATES
▸Full report

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

Recall #:
87953
Lot/product code:
Software version: 1.24.0 SP1 or lower
Recalling firm:
Siemens Healthcare Diagnostics, Inc.
View official FDA record (opens in a new tab)
Class IIModerate risk
DrugRecalled May 5, 2021

BusPIRone Hydrochloride Tablets, USP, 15 mg, 100-count bottle, Rx only, Manufactured By: Oxford Pharmaceuticals, LLC Birmingham, Alabama 35211, NDC 69584-093-10

Presence of Foreign Tablets/Capsules

ALL 50 STATES
▸Full report

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

Recall #:
D-0602-2021
Lot/product code:
Lot #: C21021A, Exp. 03/2023
Recalling firm:
Oxford Pharmaceuticals, LLC
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled May 5, 2021

Omnera 400A Digital Radiographic System

There is the potential for the X-Ray system to short circuit due to an ingress of liquid in the display handles which may result in uncontrolled movement of the Overhead Tube Crane (OTC).

ALL 50 STATES
▸Full report

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

Recall #:
90446
Lot/product code:
UDI/DI: 07350008750012; 2001-2003, 2006-2044, 2046-2056, 2118-2126, 2128-2131, 2134-2160, 2164-2175, 2177-2195, 2197-2208, 2210-2212, 2214-2224, 2226-2236.
Recalling firm:
Arcoma AB
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled May 5, 2021

Omnera 400T Digital Radiographic System

There is the potential for the X-Ray system to short circuit due to an ingress of liquid in the display handles which may result in uncontrolled movement of the Overhead Tube Crane (OTC).

ALL 50 STATES
▸Full report

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

Recall #:
90446
Lot/product code:
UDI/DI:07350008750050; 2001-2003, 2006-2044, 2046-2056, 2118-2126, 2128-2131, 2134-2160, 2164-2175, 2177-2195, 2197-2208, 2210-2212, 2214-2224, 2226-2236.
Recalling firm:
Arcoma AB
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled May 10, 2021

Ventec Life Systems VOCSN Multi-Function Ventilator Model/Version/Catalog Number: V+O+C+S+N+Pro/English/PRT-00490-001; V+O+C+S+N+Pro/Japan/PRT-00490-100; V+C+Pro/English/PRT-00900-001; V+C+Pro/Japan/PRT-00900-100; V+C/English/PRT-01098-000; V+O+C+S+N/English/PRT-01100-000; V+O+C+S+N/English/PRT-01100-001;

Due to a component failure, ventilators may unexpectedly shut down or have a loss of blower function while in patient use. The shutdown potentially prevents the ventilator from providing ventilation therapy.

ALL 50 STATES
▸Full report

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

Recall #:
87838
Lot/product code:
Catalog Number: PRT-00490-001 GTIN (Primary ID): 00855573007792/00855573007006 Serial Numbers: 114303; 114304; 113728; 113729; 113697; 114296; 113587; 113684; 113706; 113003; 112957; 112961; 112962; 112965; 112972; 112974; 112994; 112995; 112999; 113006; 113008; 113010; 113520; 113522; 113525; 113533; 113534; 113536; 113547; 113550; 113555; 113556; 113557; 113561; 113563; 113689; 113724; 114021; 114101; 114105; 114106; 114107; 114109; 114110; 114111; 114116; 114117; 114310; 114333; 114108; 112792; 112798; 114497; 114324; 114325; 114330; 114336; 114493; 114537; 113046; 113662; 113667; 113682; 113591; 113594; 113654; 113655; 113740; 114020; 114030; 114044; 114046; 114048; 114096; 114114; 114019; 114025; 114027; 114033; 114039; 114040; 114045; 114051; 114028; 113704; 113746; 113748; 113753; 113760; 113061; 113725; 113586; 113691; 114307; 114309; 113028; 113066; 113539; 113515; 113709; 114047; 112814; 112824; 112829; 112830; 112844; 112848; 112865; 112866; 112807; 112822; 112823; 112834; 112835; 112847; 112854; 112876; 122848; 113758; 114508; 114951; 114342; 114343; 114346; 114351; 114360; 114500; 114345; 114499; 114505; 112976; 113037; 113040; 113524; 114322; 114498; 114510; 114636; 114640; 114641; 114676; 114685; 114695; 114701; 114820; 114827; 114841; 114900; 114901; 114674; 114725; 114800; 114810; 114812; 114822; 114825; 113057; 113063; 112821; 112839; 112842; 112867; 112826; 112837; 112825; 112982; 112987; 113510; 113511; 113546; 113584; 113592; 113652; 113686; 113710; 113723; 113756; 113671; 113675; 113715; 114009; 114013; 114489; 114494; 113549; 113744; 114637; 114947; 112765; 112766; 112767; 112768; 112770; 112774; 112775; 112776; 112778; 112779; 112780; 112787; 112815; 112841; 112862; 112968; 112977; 113013; 113014; 113016; 113017; 113018; 113027; 113032; 113039; 113050; 113535; 113562; 113588; 113658; 113755; 114032; 114488; 114842; AARC0001; AARC002; AARC003; AARC004; AARC005; AARC006; AARC007; AARC008; AARC009; 114095; 113590;  Catalog Number: PRT-00490-100 GTIN (Primary ID): 00855573007761/00855573007204 Serial Numbers: 112929; 113598; 113233; 113238; 113239; 113241; 113243; 113244; 113245; 113603; 114193; 114201; 114255; 114266;  Catalog Number: PRT-00900-001 GTIN (Primary ID): 00855573007778/00855573007433 Serial Numbers: 113365; 113405; 113906; 113962; 113407; 113414; 113430; 113390; 113437; 113262; 113380; 113458; 113384; 113398; 113442; 113858; 113441; 113443; 113445; 113915; 113817; 113898; 113899; 113378; 113395; 113923; 113972; 113937; 113945; 113957; 113961; 113968; 113368; 113373; 113379; 113264; 113351; 113389; 113370; 113377; 113454; 113468; 113804; 113823; 113830; 113837; 113838; 113881; 113882; 113888; 113892; 113902; 113927; 113967; 113399;  Catalog Number: PRT-00900-100 GTIN (Primary ID): 00855573007785 Serial Numbers: 113096; 113300; 112923; 113107; 112877; 110392; 113143; 113183; 113274; 113323;  Catalog Number: PRT-01098-000 GTIN (Primary ID): 00855573007730 Serial Numbers: 114444; 114451; 114615; 114226; 114442; 114450; 114452; 114441; 114453;  Catalog Number: PRT-01100-000 GTIN (Primary ID): 00855573007747 Serial Numbers: 114556; 114591; 114634; 114771; 114779; 114603; 114606; 114667; 114710; 114713; 114737; 114739; 114559; 114783; 114869; 114576; 114587; 114364; 114369; 114374; 114387; 114391; 114560; 114568; 114764; 114776; 114787; 114849; 114549; 114569; 114705; 114562; 114355; 114372; 114405; 114550; 114594; 114601; 114652; 114659; 114661; 114662; 114358; 114383; 114386; 114389; 114390; 114530; 114540; 114401; 114422; 114424; 114548; 114670; 114714; 114850; 114414; 114417; 114554; 114561; 114861; 114862; 114543; 114786; 114789; 114912; 114917; 114851; 114628; 114211; 114542; 114528; 114531; 114483; 114750; 114643; 114644; 114748; 114926; 114991; 114891; 114892; 114894; 114357; 114409; 114604; 114413; 114653; 114654; 114734; 114754;  Catalog Number: PRT-01100-001 GTIN (Primary ID): 00855573007747 Serial Numbers: 114965; 114966; 114967;
Recalling firm:
Ventec Life Systems, Inc.
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled May 11, 2021

Skyton Bracket Flatscreen, Revision 2 & 3-The FS32 is a single monitor mounting bracket intended for use with a 32 inch (maximum) flat screen monitor. Model: FS32

Failure of the FS32 Monitor Brackets from the mounting block could potentially loosen over time and eventually detach from the baseplate, result in the display interface dismounting from its attachment point, causing injury to patients or staff

ALL 50 STATES
▸Full report

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

Recall #:
87939
Lot/product code:
Serial Numbers: 1504-314-00-1-0002 up to 2006-314-00-1-0185 ***UPDATED 12/10/21*** Recall expanded to include Rev 3. Complete list of recalled Serial Numbers: 1504-314-00-1-0002 1504-314-00-1-0003 1504-314-00-1-0004 1508-314-00-1-0005 1508-314-00-1-0006 1508-314-00-1-0007 1508-314-00-1-0008 1509-314-00-1-0009 1509-314-00-1-0010 1509-314-00-1-0011 1509-314-00-1-0012 1510-314-00-1-0013 1510-314-00-1-0014 1601-314-00-1-0016 1601-314-00-1-0017 1610-314-00-1-0018 1610-314-00-1-0019 1610-314-00-1-0020 1610-314-00-1-0021 1610-314-00-1-0022 1610-314-00-1-0023 1610-314-00-1-0024 1610-314-00-1-0025 1610-314-00-1-0026 1610-314-00-1-0027 1610-314-00-1-0028 1610-314-00-1-0029 1610-314-00-1-0030 1610-314-00-1-0031 1610-314-00-1-0032 1802-314-00-1-0033 1802-314-00-1-0034 1802-314-00-1-0035 1802-314-00-1-0036 1802-314-00-1-0037 1802-314-00-1-0038 1802-314-00-1-0039 1802-314-00-1-0040 1802-314-00-1-0041 1802-314-00-1-0042 1803-314-00-1-0043 1803-314-00-1-0044 1803-314-00-1-0045 1803-314-00-1-0046 1803-314-00-1-0047 1803-314-00-1-0048 1803-314-00-1-0049 1803-314-00-1-0050 1803-314-00-1-0051 1803-314-00-1-0052 1809-314-00-1-0053 1809-314-00-1-0054 1809-314-00-1-0055 1809-314-00-1-0056 1809-314-00-1-0057 1809-314-00-1-0058 1809-314-00-1-0059 1809-314-00-1-0060 1809-314-00-1-0061 1809-314-00-1-0062 1809-314-00-1-0063 1809-314-00-1-0064 1810-314-00-1-0065 1810-314-00-1-0066 1810-314-00-1-0067 1810-314-00-1-0068 1810-314-00-1-0069 1810-314-00-1-0070 1811-314-00-1-0071 1811-314-00-1-0072 1811-314-00-1-0073 1811-314-00-1-0074 1811-314-00-1-0075 1811-314-00-1-0076 1811-314-00-1-0077 1811-314-00-1-0078 1811-314-00-1-0079 1811-314-00-1-0080 1811-314-00-1-0083 1811-314-00-1-0084 1811-314-00-1-0085 1811-314-00-1-0087 1811-314-00-1-0088 1811-314-00-1-0089 1811-314-00-1-0090 1901-314-00-1-0091 1901-314-00-1-0092 1901-314-00-1-0093 1901-314-00-1-0094 1901-314-00-1-0095 1901-314-00-1-0096 1901-314-00-1-0097 1901-314-00-1-0098 1901-314-00-1-0099 1901-314-00-1-0100 1901-314-00-1-0101 1901-314-00-1-0102 1901-314-00-1-0103 1901-314-00-1-0104 1901-314-00-1-0105 1901-314-00-1-0106 1901-314-00-1-0107 1901-314-00-1-0108 1901-314-00-1-0109 1904-314-00-1-0121 1904-314-00-1-0127 2005-314-00-1-0131 2005-314-00-1-0132 2005-314-00-1-0133 2005-314-00-1-0134 2005-314-00-1-0135 2005-314-00-1-0136 2005-314-00-1-0137 2005-314-00-1-0138 2005-314-00-1-0139 2005-314-00-1-0140 2005-314-00-1-0141 2005-314-00-1-0142 2006-314-00-1-0143 2006-314-00-1-0144 2006-314-00-1-0145 2006-314-00-1-0146 2011-314-00-2-0002 2011-314-00-2-0003 2011-314-00-2-0004 2011-314-00-2-0005 2011-314-00-2-0006 2011-314-00-2-0007 2011-314-00-2-0008 2011-314-00-2-0009 2011-314-00-2-0010 2011-314-00-2-0011 2011-314-00-2-0012 2011-314-00-2-0013 2011-314-00-2-0014 2011-314-00-2-0015 2011-314-00-2-0016 2011-314-00-2-0017 2011-314-00-2-0018 2011-314-00-2-0019 2011-314-00-2-0020 2011-314-00-2-0021 2011-314-00-2-0022 2011-314-00-2-0023 2011-314-00-2-0024 2011-314-00-2-0025 2011-314-00-2-0026 2011-314-00-2-0027 2011-314-00-2-0028 2011-314-00-2-0029 2011-314-00-2-0030 2011-314-00-2-0031 2011-314-00-2-0032 2011-314-00-2-0033 2011-314-00-2-0034 2011-314-00-2-0035 2011-314-00-2-0036 2011-314-00-2-0037 2011-314-00-2-0038 2011-314-00-2-0039 2011-314-00-2-0040 2011-314-00-2-0041 2011-314-00-2-0042 2011-314-00-2-0043 2011-314-00-2-0044 2011-314-00-2-0045 2011-314-00-2-0046 2011-314-00-2-0047 2011-314-00-2-0048 2011-314-00-2-0049 2011-314-00-2-0050 2011-314-00-2-0051 2011-314-00-2-0052 2011-314-00-2-0053 2011-314-00-2-0054 2011-314-00-2-0055 2011-314-00-2-0056 2011-314-00-2-0057 2011-314-00-2-0058 2011-314-00-2-0059 2011-314-00-2-0060 2011-314-00-2-0061 2011-314-00-2-0062 2011-314-00-2-0063 2011-314-00-2-0064 2011-314-00-2-0065 2011-314-00-2-0066 2011-314-00-2-0067 2011-314-00-2-0068 2011-314-00-2-0069 2011-314-00-2-0070 2011-314-00-2-0071 2011-314-00-2-0072 2011-314-00-2-0073 2011-314-00-2-0074 2011-314-00-2-0075 2011-314-00-2-0076 2011-314-00-2-0077 2011-314-00-2-0078 2011-314-00-2-0079 2011-314-00-2-0080 2011-314-00-2-0081 2011-314-00-2-0082 2011-314-00-2-0083 2011-314-00-2-0084 2011-314-00-2-0085 2011-314-00-2-0086 2011-314-00-2-0087 2011-314-00-2-0088 2011-314-00-2-0089 2011-314-00-2-0090 2011-314-00-2-0091 2011-314-00-2-0092 2011-314-00-2-0093 2011-314-00-2-0094 2011-314-00-2-0095 2011-314-00-2-0096 2011-314-00-2-0097 2011-314-00-2-0098 2011-314-00-2-0099 2011-314-00-2-0100 2011-314-00-2-0101 2011-314-00-2-0102 2011-314-00-2-0103 2011-314-00-2-0104 2011-314-00-2-0105 2011-314-00-2-0106 2011-314-00-2-0107 2011-314-00-2-0108 2011-314-00-2-0109 2011-314-00-2-0110 2011-314-00-2-0111 2011-314-00-2-0112 2011-314-00-2-0113 2011-314-00-2-0114 2011-314-00-2-0115 2011-314-00-2-0116 2011-314-00-2-0117 2011-314-00-2-0118 2011-314-00-2-0119 2011-314-00-2-0120 2011-314-00-2-0121 2011-314-00-2-0122 2011-314-00-2-0123 2011-314-00-2-0124 2011-314-00-2-0125 2011-314-00-2-0126 2011-314-00-2-0127 2011-314-00-2-0128 2011-314-00-2-0129 2011-314-00-2-0130 2011-314-00-2-0131 2011-314-00-2-0132 2011-314-00-2-0133 2011-314-00-… (truncated, 5576 characters total — see the official FDA record for the full value)
Recalling firm:
Skytron, Div. The KMW Group, Inc
View official FDA record (opens in a new tab)
Class IIModerate risk
DrugRecalled May 11, 2021

Imperia Elita Vitaccino Coffee, 10 g sachets, 15 sachets per box, Global Beauty Technologies, Manufactured for: Imperia-Elita Ltd. & Co, KG D- 35435 Wettenberg

Marketed without an approved NDA/ANDA: FDA analysis determined presence of the pharmaceutical ingredients Sibutramine and Fluoxetine

ALL 50 STATES
▸Full report

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

Recall #:
D-0628-2021
Lot/product code:
All Lots
Recalling firm:
DASH XCLUSIVE
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled May 11, 2021

Humeral Augmented Tray (HAT) trials that are components of KIT-321HAT. Each tray contains 1 of each of the following catalog numbers for a total of 6 trials/tray: (1) HAT STD Left Tray Trial, Cat. #321-00-01; (2) HAT STD Right Tray Trial, Cat. #321-00-02; (3) HAT LAT Left Tray Trial, Cat. #321-00-11; (4) HAT LAT Right Tray Trial, Cat. #321-00-12; (5) HAT EXT LAT Left Trial, Cat. #321-00-21; and (6) HAT EXT LAT Right Trial, Cat. #321-00-22. The Humeral Augmented Tray is designed to function with the Equinoxe Reverse Shoulder System orthopedic implant components.

The HAT trial contains a retaining ring that has shown the potential to disengage during use.

ALL 50 STATES
▸Full report

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

Recall #:
87989
Lot/product code:
(1) HAT STD Left Tray Trial, Lot #279244001, UDI 10885862541239 ; (2) HAT STD Right Tray Trial, Lot #279244002, UDI 10885862541246 ; (3) HAT LAT Left Tray Trial, Lot #279244017, UDI 10885862541253; (4) HAT LAT Right Tray Trial, Lot #279244004, UDI 10885862541260; (5) HAT EXT LAT Left Trial, Lot #279244005, UDI 10885862541277; and (6) HAT EXT LAT Right Trial, Lot #279244006, UDI 10885862541284.
Recalling firm:
Exactech, Inc.
View official FDA record (opens in a new tab)
Class IHigh risk
DrugChemicalRecalled May 12, 2021

MEDICALLY MINDED Hand Sanitizer Gel, ANTIMICROBIAL FORMULA, (Ethyl Alcohol 70% v/v), 8.5 FL OZ / 250 mL bottle, Made in Mexico, Distributed by SBL Brands, LLC Las Vegas, NV 89119. UPC: 6 76753 00359 1

Chemical Contamination: FDA analysis found 1 lot of MEDICALLY MINDED Hand Sanitizer Gel, ANTIMICROBIAL FORMULA (ethyl alcohol 70%) to be below the label claim for ethanol content and to contain methanol.

ALL 50 STATES
▸Full report

The most serious kind of recall. Using this product could cause serious health problems or death.

Recall #:
D-0781-2021
Lot/product code:
Lot No: E082020, "Best Buy": 5/21/2022
Recalling firm:
Global Sanitizers LLC
View official FDA record (opens in a new tab)
Class IIModerate risk
DrugRecalled May 12, 2021

MEDICALLY MINDED Hand Sanitizer Gel, ANTIMICROBIAL FORMULA, (Ethyl Alcohol 70% v/v), 8.5 FL OZ (250 mL) bottle, Manufactured by Asiaticon, S.A. de C.V. Conkal 62, Jardines del Ajusco, Tlalpan, Ciudad de Mexico, C.P. 14200, Distributed by SBL Brands, LLC. Las Vegas, NV 89119. Made in Mexico UPC 6 76753 00414 7

CGMP Deviations: lots and products of hand sanitizer are being recalled because they were manufactured under the same conditions as the product lot found to contain methanol.

ALL 50 STATES
▸Full report

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

Recall #:
D-0779-2021
Lot/product code:
Lot No: E372020, "Best Buy": 5/21/2022;
Recalling firm:
Global Sanitizers LLC
View official FDA record (opens in a new tab)
Class IIModerate risk
DrugRecalled May 12, 2021

MEDICALLY MINDED ANTIMICROBIAL Hand Sanitizer Gel with Aloe Vera, (Ethyl Alcohol 70% v/v), 10 FL OZ / 300 mL, Manufactured by Grupo V-Klean S.A. de C.V, Calle Alborada 124, Parques del Pedregal, Tlalpan, 14250 Ciudad de Mexico, CDMX, Distributed by SBL Brands, LLC. Las Vegas, NV 89119. Made in Mexico UPC: 6 76753 00417 8

CGMP Deviations: lots and products of hand sanitizer are being recalled because they were manufactured under the same conditions as the product lot found to contain methanol.

ALL 50 STATES
▸Full report

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

Recall #:
D-0778-2021
Lot/product code:
Lot No: GV4420205 Best By, 5/21/2022
Recalling firm:
Global Sanitizers LLC
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled May 12, 2021

CardioQuip, Modular Cooler-Heater 1000(m),Compact Unit, Model:MCH-1000(m),CE 2797, UDI: (01)00860000846110

Labeling does not include guidance for proper water-quality maintenance and device inspection for heater cooler devices.

ALL 50 STATES
▸Full report

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

Recall #:
88622
Lot/product code:
All Serial numbers
Recalling firm:
CardioQuip, LLC
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled May 12, 2021

CardioQuip, Modular Cooler-Heater, Model: MCH-1000(i), CE 2797, UDI: (01)00860000846103

Labeling does not include guidance for proper water-quality maintenance and device inspection for heater cooler devices.

ALL 50 STATES
▸Full report

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

Recall #:
88622
Lot/product code:
All Serial numbers
Recalling firm:
CardioQuip, LLC
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled May 12, 2021

CardioQuip, Modular Cooler-Heater 1000(i), Standard Unit, Model: MCH-10RMS, CE 2797, UDI: (01) 00860000846127

Labeling does not include guidance for proper water-quality maintenance and device inspection for heater cooler devices.

ALL 50 STATES
▸Full report

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

Recall #:
88622
Lot/product code:
All Serial numbers
Recalling firm:
CardioQuip, LLC
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled May 12, 2021

IsoGel Air - support surface assists in the prevention and treatment of all pressure ulcers stages, Model Number 2860, Part 2860000999

Medical devices intended for use in a healthcare facility were distributed to residential customers and may be in use in a home environment. The product s labeling accurately identifies the correct use environment, but home users may not be aware of or fully understand these instructions intended for healthcare professionals

ALL 50 STATES
▸Full report

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

Recall #:
88199
Lot/product code:
Serial Numbers:  031528600216109 051428600212599 081328600206460 UDI: 07613327298512
Recalling firm:
Stryker Medical Division of Stryker Corporation
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled May 12, 2021

DJO Surgical EMPOWR 3D Knee Tibial Insert - e-plus, REF: 341-16-711 Left Sz. 11 16mm, CE 0086, Sterile H2O2, UDI: (01)00888912167185

Packaging mixup; There is a potential that packaging identified as 12mm knee prosthesis contains 16mm knee prosthesis and 16mm knee prosthesis packaging contains 12 mm knee prosthesis.

ALL 50 STATES
▸Full report

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

Recall #:
87942
Lot/product code:
Lot # 155T1035
Recalling firm:
Encore Medical, LP
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled May 12, 2021

Surgistool-intended to support a healthcare professional during surgical procedures Model 830, Part Number 0830000000

Medical devices intended for use in a healthcare facility were distributed to residential customers and may be in use in a home environment. The product s labeling accurately identifies the correct use environment, but home users may not be aware of or fully understand these instructions intended for healthcare professionals

ALL 50 STATES
▸Full report

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

Recall #:
88199
Lot/product code:
Serial Numbers: 1202033898 1206032470 1406034563 1607037109   UDI (DI#): 07613327282566
Recalling firm:
Stryker Medical Division of Stryker Corporation
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled May 12, 2021

Stretcher Chair-for use in all acute care hospitals and medical outpatient services Model Number: 5050 Part # 5050000000

Medical devices intended for use in a healthcare facility were distributed to residential customers and may be in use in a home environment. The product s labeling accurately identifies the correct use environment, but home users may not be aware of or fully understand these instructions intended for healthcare professionals

ALL 50 STATES
▸Full report

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

Recall #:
88199
Lot/product code:
Serial Numbers:  N/A UDI: 07613327282511
Recalling firm:
Stryker Medical Division of Stryker Corporation
View official FDA record (opens in a new tab)