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FDA food · drug · device recalls, merged

Before you eat it, take it, or plug it in — check.

Big Nope pulls three separate FDA recall feeds into one list per state, so you’re not searching three government databases to get one answer.

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)

Recalls nationwide

Data last updated: September 9, 2026 at 1:18 PM UTC

19,424 recalls found
Wording
Class IHigh risk
FoodBacteria/virusRecalled May 1, 2026

#0083004 Ranch Seasoning, Net Wt: 25 lbs. JCB Flavors, 1224 Clark St. Watertown, WI 53094.

Products may be potentially contaminated with Salmonella.

Full report

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

Recall #:
H-0889-2026
Lot/product code:
Lot# 087002-2-1
Recalling firm:
JCB Flavors, LLC
View official FDA record (opens in a new tab)
Class IHigh risk
FoodBacteria/virusRecalled May 1, 2026

#800414/003729Butter Parsley, Net Wt: 50 lbs. JCB Flavors, 1224 Clark St. Watertown, WI 53094

Products may be potentially contaminated with Salmonella.

Full report

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

Recall #:
H-0885-2026
Lot/product code:
Lot: 087735-1-1
Recalling firm:
JCB Flavors, LLC
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled May 1, 2026

CGuard Prime Carotid Stent System, 135cm, 10mmx30mm Model/Catalog Number: CND1030

Stent delivery system may encounter complications during deployment which may result in high resistance or inability to deploy the stent.

ALL 50 STATES
Full report

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

Recall #:
98922
Lot/product code:
UDI: 07290120281776; all lots/serial numbers manufactured between 02/03/2025 and 02/23/2026
Recalling firm:
INSPIREMD Inc
View official FDA record (opens in a new tab)
Class IHigh risk
FoodBacteria/virusRecalled May 1, 2026

Popping Topping, Sour Cream & Onion Flavored Popcorn Seasoning, Net Wt: 1.6oz. UPC 0 31851-01001 6. Distributed By: Butler's Pantry, 1224 Clark St. Watertown, WI 53094.

Products may be potentially contaminated with Salmonella.

Full report

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

Recall #:
H-0886-2026
Lot/product code:
Lot: 057596
Recalling firm:
JCB Flavors, LLC
View official FDA record (opens in a new tab)
Class IHigh risk
FoodBacteria/virusRecalled May 1, 2026

#007560 Fiery Hot Seasoning (Reduced Salt), Net Wt: 25 lbs. JCB Flavors, 1224 Clark Street, Watertown, WI 53094

Products may be potentially contaminated with Salmonella.

Full report

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

Recall #:
H-0881-2026
Lot/product code:
Lot: 087861-1-1
Recalling firm:
JCB Flavors, LLC
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled May 1, 2026

CGuard Prime Carotid Stent System, 135cm, 9mx30mm Model/Catalog Number: CND0930

Stent delivery system may encounter complications during deployment which may result in high resistance or inability to deploy the stent.

ALL 50 STATES
Full report

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

Recall #:
98922
Lot/product code:
UDI: 07290120281738; all lots/serial numbers manufactured between 02/03/2025 and 02/23/2026
Recalling firm:
INSPIREMD Inc
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled May 1, 2026

Giraffe OmniBed, a combination of an infant incubator and an infant warmer, All Models

GE HealthCare has become aware of a potential issue involving the canopy soffit beneath the control panel end of the device. Under certain conditions, for example, impact during transport, one or more of the fasteners that secure the soffit can disengage. If this occurs, a fastener could fall into the patient compartment. In rare circumstances, if multiple fasteners disengage, the canopy soffit can become loose or detach. These conditions could potentially result in patient injury.

ALL 50 STATES
Full report

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

Recall #:
98986
Lot/product code:
Serial Numbers: HDGP50034 HDGP51018 HDGS50069 HDGS50070 HDGS50074 HDGS50077 HDGS50158 HDGS50162 HDGS52245 HDGS52286 HDGT50374 HDGT50399 HDGS50464 HDGS50560 HDGS50569 HDGS50570 HDGD50349 HDGG54079 HDGJ50278 HDGJ50281 HDGJ50390 HDGJ50391 HDGJ50394 HDGJ50400 HDGK52363 HDGM50481 HDGM50482 HDGM50483 HDGM50484 HDGM50485 HDGM50486 HDGQ50625 HDGQ50626 HDGQ50627 HDGQ50628 HDGQ50629 HDGS50369 HDGS50370 HDGS50371 HDGS50372 HDGR50086 HDGL51597 HDGG54268 HDGG54270 HDGG54410 HDGK51696 HDGL51002 HDGL51003 HDGL51004 HDGL51005 HDGL51032 HDGN50383 HDGP50522 HDGQ50763 HDGQ50882 HDGQ50884 HDGQ50886 HDGQ50887 HDGQ50901 HDGQ50902 HDGQ50903 HDGQ50904 HDGQ50905 HDGQ50906 HDGQ50907 HDGQ50908 HDGQ50909 HDGQ50910 HDGQ50911 HDGQ50912 HDGQ50913 HDGQ50917 HDGS51833 HDGU60609 HDGU60732 HDGE50297 HDGE50370 HDGE50371 HDGK51791 HDGK51792 HDGK51793 HDGK51794 HDGK51795 HDGK51804 HDGK51822 HDGK51840 HDGR50087 HDGR50088 HDGR50178 HDGR50180 HDGR50184 HDGR50185 HDGN50863 HDGN50864 HDGN50865 HDGN50866 HDGN50868 HDGN50869 HDGN50870 HDGH60335 HDGH60316 HDGH60319 HDGH60320 HDGH60321 HDGH60322 HDGH60323 HDGH60324 HDGH60326 HDGH60327 HDGH60328 HDGH60329 HDGH60330 HDGH60331 HDGH60333 HDGH60334 HDGH60403 HDGH60407 HDGH60408 HDGH60409 HDGN50867 HDGT50420 HDGK51412 HDGK51706 HDGK52164 HDGL50039 HDGL51294 HDGL51483 HDGL51486 HDGM51574 HDGM51575 HDGM51583 HDGP51029 HDGS52343 HDGS52358 HDGJ50055 HDGN50393 HDGM50726 HDGM50093 HDGM50146 HDGM50149 HDGM50151 HDGP51237 HDGP51290 HDGP51297 HDGQ51823 HDGQ51947 HDGJ51132 HDGJ51133 HDGJ51134 HDGJ51136 HDGJ51142 HDGJ51176 HDGJ51177 HDGJ51180 HDGJ51181 HDGJ51182 HDGJ51189 HDGJ51190 HDGL50080 HDGL50082 HDGL50123 HDGL50165 HDGR52333 HDGS50800 HDGS50812 HDGU60084 HDGU60087 HDGU60098 HDGU60157 HDGU60158 HDGU60162 HDGU60168 HDGU60598 HDGT50753 HDGT50754 HDGT50756 HDGT50757 HDGU60516 HDGU60520 HDGU60523 HDGU60527 HDGU60528 HDGU60533 HDGU60535 HDGU60540 HDGU60542 HDGU60543 HDGJ51045 HDGJ51079 HDGQ50791 HDGR52718 HDGR52936 HDGL51165 HDGL51190 HDGM51272 HDGM51289 HDGN51296 HDGN51337 HDGP50832 HDGP50839 HDGT50381 HDGT50382 HDGL51672 HDGN51051 HDGN51096 HDGR50127 HDGR50143 HDGS50619 HDGS50624 HDGS50629 HDGS50630 HDGG55016 HDGJ50424 HDGJ50427 HDGJ50432 HDGK52226 HDGM50995 HDGM50996 HDGM51000 HDGM51003 HDGM51005 HDGM51009 HDGQ50958 HDGQ50961 HDGQ50963 HDGQ50965 HDGQ50967 HDGR52148 HDGR52150 HDGR52152 HDGR52221 HDGR52246 HDGR52281 HDGR52301 HDGR52310 HDGR52329 HDGR52331 HDGD00113 HDGF50369 HDGF53069 HDGF53072 HDGG55175 HDGH60780 HDGH60781 HDGJ50183 HDGJ50935 HDGJ51027 HDGK51849 HDGM50511 HDGQ51811 HDGS50516 HDGT60443 HDGT60444 HDGT60445 HDGK52275 HDGM50360 HDGM50366 HDGM50374 HDGM50397 HDGM50402 HDGM50416 HDGM50417 HDGM50430 HDGM50438 HDGM50439 HDGM50441 HDGM50448 HDGM50455 HDGM50456 HDGM50473 HDGM50548 HDGM50550 HDGM50552 HDGM50553 HDGM50554 HDGM50555 HDGM50557 HDGM50562 HDGM50564 HDGM50581 HDGM50583 HDGM50595 HDGM50632 HDGM50633 HDGM50634 HDGM50635 HDGM50641 HDGM50642 HDGM50646 HDGM50648 HDGM50649 HDGM50650 HDGM50681 HDGM50686 HDGS52298 HDGM50445 HDGM50643 HDGL50363 HDGL51839 HDGK51331 HDGK51348 HDGL51846 HDGL51847 HDGQ51109 HDGQ51112 HDGQ51116 HDGQ51117 HDGS50785 HDGS50787 HDGS52365 HDGS52369 HDGT60089 HDGT60113 HDGL50427 HDGL50628 HDGS50005 HDGS50010 HDGN50437 HDGN50586 HDGN50588 HDGN50590 HDGN50591 HDGN50592 HDGN50593 HDGN50594 HDGN50606 HDGN50793 HDGG54096 HDGG54099 HDGG54100 HDGL51851 HDGL51857 HDGL51858 HDGP50025 HDGQ51891 HDGT50691 HDGM50788 HDGM50789 HDGN50790 HDGH61006 HDGS50355 HDGS50755 HDGH60898 HDGE50352 HDGJ50127 HDGJ50133 HDGJ50393 HDGJ50396 HDGJ50397 HDGJ50399 HDGJ50401 HDGJ50404 HDGJ50405 HDGT50740 HDGJ50654 HDGJ50657 HDGG54196 HDGH60133 HDGH60485 HDGH60505 HDGH60571 HDGJ50175 HDGK51252 HDGK51350 HDGS51933 HDGS51974 HDGS52066 HDGS52088 HDGS52149 HDGS52151 HDGK51230 HDGK51232 HDGK52080 HDGK52081 HDGK52189 HDGK52190 HDGK52194 HDGK52195 HDGK52263 HDGN51268 HDGN51306 HDGN51308 HDGJ51212 HDGL51827 HDGM51259 HDGM51356 HDGM51360 HDGN50309 HDGP50101 HDGU60725 HDGU60731 HDGU60735 HDGU60840 HDGU60863 HDGU60881 HDGU63034 HDGU63201 HDGU63220 HDGU63222 HDGQ50008 HDGQ50079 HDGU60441 HDGM52234 HDGN50198 HDGP50027 HDGP50031 HDGP50032 HDGP50048 HDGP50050 HDGP50053 HDGP50055 HDGP50057 HDGP50073 HDGP50075 HDGP50077 HDGP50083 HDGP50084 HDGP50087 HDGP50089 HDGP50092 HDGP50110 HDGP50111 HDGP50112 HDGP50114 HDGP50115 HDGP50118 HDGP50122 HDGP50127 HDGL51643 HDGL51802 HDGM50104 HDGM50131 HDGM50133 HDGM50137 HDGM50138 HDGM50139 HDGM50140 HDGM50142 HDGM50143 HDGM50144 HDGS50191 HDGS50200 HDGS50780 HDGT50540 HDGK52422 HDGK52604 HDGL50012 HDGL50019 HDGL50020 HDGL50106 HDGL50733 HDGM50465 HDGM50663 HDGM50664 HDGM50702 HDGP51156 HDGQ51070 HDGQ51711 HDGS51245 HDGS51585 HDGS51588 HDGS51592 HDGS51593 HDGS51595 HDGS51600 HDGS51604 HDGS52370 HDGS52377 HDGS52380 HDGS52384 HDGS52385 HDGG54025 HDGH60268 HDGN50587 HDGN50598 HDGQ51194 HDGU60074 HDGU60075 HDGV60169 HDGE50372 HDGG54306 HDGG55066 HDGM51909 HDGL51449 HDGN50490 HDGQ50500 HDGQ51524 HDGQ51722 HDGQ51723 HDGQ51724 HDGQ51725 HDGQ51726 HDGQ51727 HDGQ51728 HDGQ51729 HDGQ51730 HDGQ51732 HDGT60589 HDGT… (truncated, 195891 characters total — see the official FDA record for the full value)
Recalling firm:
GE Medical Systems, LLC
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled May 1, 2026

Brand Name: CGuard Prime Carotid Stent System, 135cm, 8mmx30mm Model/Catalog Number: CND0830

Stent delivery system may encounter complications during deployment which may result in high resistance or inability to deploy the stent.

ALL 50 STATES
Full report

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

Recall #:
98922
Lot/product code:
UDI: 07290120281691; all lots/serial numbers manufactured between 02/03/2025 and 02/23/2026
Recalling firm:
INSPIREMD Inc
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled May 1, 2026

Giraffe OmniBed Field Replaceable Unit (FRU), Model Numbers 6600-1056-400 and 6600-1461-500

GE HealthCare has become aware of a potential issue involving the canopy soffit beneath the control panel end of the device. Under certain conditions, for example, impact during transport, one or more of the fasteners that secure the soffit can disengage. If this occurs, a fastener could fall into the patient compartment. In rare circumstances, if multiple fasteners disengage, the canopy soffit can become loose or detach. These conditions could potentially result in patient injury.

ALL 50 STATES
Full report

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

Recall #:
98986
Lot/product code:
Serial Numbers: 5452896 801057486 800977619 801093759 5584569 5587625 5367527 5603110 5371240 5497382
Recalling firm:
GE Medical Systems, LLC
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled April 30, 2026

Brand Name: CORFLO Product Name: CORFLO* Safety PEG Kit Model/Catalog Number: 30-4320

Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets.

ALL 50 STATES
Full report

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

Recall #:
98907
Lot/product code:
UDI-DI 10350770007585, Lot Numbers 30365226 and 30382750
Recalling firm:
Avanos Medical, Inc.
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled April 30, 2026

Product Name: MIC Safety Percutaneous Endoscopic Gastrostomy PEG Kit 24 Fr PUSH OTW Model/Catalog Number: 7170-24 Product Description: Feeding Tube Kit Component: No

Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets.

ALL 50 STATES
Full report

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

Recall #:
98907
Lot/product code:
UDI-DI: 10350770007790, Lot Numbers 30370715, 30371329, 30375466
Recalling firm:
Avanos Medical, Inc.
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled April 30, 2026

Surgify Halo, 4.0 mm, Short, Model/Catalog Number: 40.070.NVG.U1; drills, burrs, trephines & accessories (simple, powered)

Potential for burr breakage, occurring during bi-portal endoscopic spinal surgery (BESS).

ALL 50 STATES
Full report

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

Recall #:
98918
Lot/product code:
UDI: 06429811532267; All lots until the IFU update has been implemented
Recalling firm:
SURGIFY MEDICAL OY
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled April 30, 2026

Surgify Halo, 5.4 mm, Long, Model/Catalog Number: 54.125.NVG.U1; drills, burrs, trephines & accessories (simple, powered)

Potential for burr breakage, occurring during bi-portal endoscopic spinal surgery (BESS).

ALL 50 STATES
Full report

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

Recall #:
98918
Lot/product code:
UDI: 06429811532304 ; All lots until the IFU update has been implemented
Recalling firm:
SURGIFY MEDICAL OY
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled April 30, 2026

Product Name: MIC Safety Percutaneous Endoscopic Gastrostomy PEG Kit 20 Fr PUSH OTW Model/Catalog Number: 7170-20 Product Description: Feeding Tube Kit Component: No

Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets.

ALL 50 STATES
Full report

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

Recall #:
98907
Lot/product code:
Lot Code: Model No 7170-20, UDI-DI 10350770007776, Lot Numbers 30370714, 30373419, 30374048, 30378746
Recalling firm:
Avanos Medical, Inc.
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled April 30, 2026

Product Name: CORFLO* Safety PEG Kit with ENFit Connector Model/Catalog Number: 50-5320

Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets.

ALL 50 STATES
Full report

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

Recall #:
98907
Lot/product code:
UDI-DI 10350770007516, Lot Numbers 30365231, 30371022, 30373824, 30378385, 30383807, 30385321
Recalling firm:
Avanos Medical, Inc.
View official FDA record (opens in a new tab)
Class IHigh risk
FoodBacteria/virusRecalled April 30, 2026

Malazi 100% PURE SUDANESE SESAME Tahina G.W.: 1K.g UPC 6 224011 088244 Produced by: AL-MALAZ COMPANY FOR TRADE AND INDUSTRY Piece No. 110-250 acres area Badr City - Egypt

Salmonella. The firm was notified by the North Carolina Department of Agriculture that the product test positive for Salmonella.

Full report

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

Recall #:
H-0860-2026
Lot/product code:
PROD: 31/12/2024 EXP: 30/12/2026
Recalling firm:
Nassar Investment Company LLC
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled April 30, 2026

BD Pyxis MedStation ES Tower REF: 352 Medication cabinet

Fingerprint scanner may overheat to a temperature to cause 1st degree burn.

ALL 50 STATES
Full report

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

Recall #:
98895
Lot/product code:
All Serial Numbers/UDI:10885403512674
Recalling firm:
CareFusion 303, Inc.
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled April 30, 2026

Product Name: MIC Safety Percutaneous Endoscopic Gastrostomy PEG Kit with ENFit Connectors 24 Fr PUSH OTW Model/Catalog Number: 8170-24

Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets.

ALL 50 STATES
Full report

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

Recall #:
98907
Lot/product code:
UDI-DI 10350770007837, Lot Numbers 30371847, 30374834, 30378748, 30380347
Recalling firm:
Avanos Medical, Inc.
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled April 30, 2026

Product Name: MIC Safety Percutaneous Endoscopic Gastrostomy PEG Kit with ENFit Connectors 14 Fr PULL Model/Catalog Number: 8180-14

Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets.

ALL 50 STATES
Full report

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

Recall #:
98907
Lot/product code:
UDI-DI 10350770007844, Lot Numbers 30371318, 30375469, 30383056
Recalling firm:
Avanos Medical, Inc.
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled April 30, 2026

directCHECK ACT-LR whole blood quality control, level 2 Model/Catalog Number: DCGLR-2

Assayed Whole blood control contains labeling with incorrect performance range.

ALL 50 STATES
Full report

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

Recall #:
98979
Lot/product code:
Lot #: A6DLA001 Unique Device Identifier: 10711234170373
Recalling firm:
Accriva Diagnostics, Inc.
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled April 30, 2026

Product Name: MIC Safety Percutaneous Endoscopic Gastrostomy PEG Kit with ENFit Connectors 14 Fr PUSH OTW Model/Catalog Number: 8170-14 Product Description: Feeding Tube Kit Component: No

Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets.

ALL 50 STATES
Full report

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

Recall #:
98907
Lot/product code:
UDI-DI 10350770007813, Lot Number 30370718
Recalling firm:
Avanos Medical, Inc.
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled April 30, 2026

BD Pyxis MedStation ES REF: 323 Medication cabinet

Fingerprint scanner may overheat to a temperature to cause 1st degree burn.

ALL 50 STATES
Full report

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

Recall #:
98895
Lot/product code:
All Serial Numbers/UDI:10885403512667
Recalling firm:
CareFusion 303, Inc.
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled April 30, 2026

TDC VELOCE", 23G Two Dimensional Cutter - 20k CPM; Article Numbers: 9268.VIT23, 9311.23G01, 9311.23G02, 9311.23K01, 9311.23K02, 9311.23K03, 9623.G0201, 9623.G0202, 9623.K0201, 9311.23G01-00;

An increase in incidence in complaints of a loose outer knife and reports of the outer knife becoming loose during use.

ALL 50 STATES
Full report

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

Recall #:
98814
Lot/product code:
1. Article Number: 9268.VIT23; UDI-DI: 08717872031866; 2. Article Number: 9311.23G01; UDI-DI: 08717872035109; 3. Article Number: 9311.23G02; UDI-DI: 08717872035338; 4. Article Number: 9311.23K01; UDI-DI: N/A; 5. Article Number: 9311.23K02; UDI-DI: N/A; 6. Article Number: 9311.23K03; UDI-DI: N/A; 7. Article Number: 9623.G0201; UDI-DI: N/A; 8. Article Number: 9623.G0202; UDI-DI: N/A; 9. Article Number: 9623.K0201; UDI-DI: N/A; 10. Article Number: 9311.23G01-00; UDI-DI: 08717872035307; Lot Numbers: 100637001, 57682-*-*-1, 64312-*-*-1, 69017-*-*-1, 73237-*-*-1, 74225-*-*-1, 75735-*-*-1, 79460-*-*-1, 80338-*-*-1, 80963-*-*-1, 81335-*-*-1, 81679-*-*-1, 82213-*-*-1, 82325-*-*-1, 82742-*-*-1, 82779-*-*-1, 83584-*-*-1, 84580-*-*-1, 85451001, 86069001, 86798001, 86799001, 87205001, 88231001, 91957001, 92629001, 92630001, 93336001, 94351001, 95436001, 95462001, 96097001, 96123001, 97279001, 97789001, 98643001, 99130001, 99185001, 99697001;
Recalling firm:
D.O.R.C. Dutch Opthalmic Research Center Intl B.V.
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled April 30, 2026

Product Name: MIC Safety Percutaneous Endoscopic Gastrostomy PEG Kit with ENFit Connectors 20 Fr PULL Model/Catalog Number: 8180-20

Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets.

ALL 50 STATES
Full report

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

Recall #:
98907
Lot/product code:
Lot Code: Model No 8180-20, UDI-DI 10350770007851, Lot Numbers 20133232, 30371326, 30378749, 30378751, 30379686, 30383063, 30383057, 80403339, 80403342
Recalling firm:
Avanos Medical, Inc.
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled April 30, 2026

Product Name: MIC Safety Percutaneous Endoscopic Gastrostomy PEG Kit with ENFit Connectors 20 Fr PUSH OTW Model/Catalog Number: 8170-20

Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets.

ALL 50 STATES
Full report

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

Recall #:
98907
Lot/product code:
UDI-DI 10350770007820, Lot Numbers 30371324, 30374833, 30384889, 80403350
Recalling firm:
Avanos Medical, Inc.
View official FDA record (opens in a new tab)