Recalls

All US Product Recalls

Searchable archive of product recalls from the FDA, USDA FSIS, CPSC, NHTSA, and EPA — translated into plain English, severity-scored from objective criteria, and always linked back to the original government notice.

How to read this listing

Every recall on this list has been scored 1–5 against an objective rubric from the agency’s own classification, presence of reported injuries or deaths, distribution scope, and hazard type. The colored severity badge on each card is the score — 5 (Critical) means the agency’s own highest classification or reported deaths or serious injuries, 4 (Severe) means significant injury or hospitalization risk, and 3 (High) means a known hazard with no confirmed harm yet. Filter to 3+ (High and above) if you want to skip routine Class-III notices.

The agency chips above control which streams are visible. FDA spans food, drugs, and medical devices. USDA FSIS is meat, poultry, and processed egg products. CPSC is household consumer products. NHTSA is vehicles, tires, and child seats. Nationwide on a card means the recall affects every US state — most do — while a state list means distribution was limited.

Click any recall to see the full summary, affected lot codes and model numbers, the agency’s own classification, and a direct link back to the original government notice for verification.

Agency

All agencies FDA (Food)FDA (Drugs)FDA (Devices)USDA FSIS CPSC NHTSA EPA

126–150 of 114834

ModerateFDA (Devices)·Z-0204-2027·2026-10-28
CooperVision recalls Softmed Breathables Advanced Toric contact lenses for labeling error
CooperVision is recalling Softmed Breathables Advanced Toric contact lenses because the packaging incorrectly states they are for extended wear, though they are only approved for daily wear.
Product
Generic Name: Softmed Breathables Advanced Toric (fanfilcon A) Soft (Hydrophilic) Contact Lens; Model/Catalog Number: Softmed Breathables Advanced Toric Product Description: 55% water content, toric, silicone hydrogel contact lens for daily wear, frequent replacement. Blister…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0263-2027·2026-10-28
Boston Scientific Recalls Defective Direxion Torqueable Microcatheters
Boston Scientific is recalling 550 Direxion Torqueable Microcatheters due to insufficient UV curing of the hydrophilic coating and raised ridges on nitinol sleeves.
Product
Direxion Torqueable Microcatheter, NGMC/TRANSEND/027/BERN/1RO/130; Material Number: M001195940
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Food)·H-0154-2027·2026-10-28
El Ruisenor De Mexico Recalls Wheat Bran for Undeclared Wheat Allergen
El Ruisenor De Mexico, Inc. is recalling wheat bran packaged in clear plastic units because it contains an undeclared wheat allergen. The product was distributed primarily in California and limited areas in other states.
Product
Wheat Bran; packaged in 1lb, 5lb, 50lb clear plastic units. No UPC
Category
Food
Distribution
7 states
ModerateFDA (Drugs)·D-0068-2027·2026-10-28
ARU Toothpaste Recalled for CGMP Deviations
Pritam International is voluntarily recalling 15,264 tubes of ARU Toothpaste due to Current Good Manufacturing Practice (CGMP) deviations.
Product
ARU, Toothpaste, Gum Health, 9 Ingredients, Soothing Mint, (stannous fluoride 0.45%) Net Wt 3.5 oz (99g), Distributed by Ashtel Studios Inc., Ontario, California 91761, NDC 84140-786-35, Item # 88786 UPC 8 10147 88786 6
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0229-2027·2026-10-28
Boston Scientific Recalls Defective Direxion Torqueable Microcatheters
Boston Scientific is recalling 358 Direxion Torqueable Microcatheters due to insufficient UV curing of the hydrophilic coating and raised ridges on nitinol sleeves.
Product
Direxion Torqueable Microcatheter, NGMC/SINGLE/021/J/1RO/105; Material Number: M001195260
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0278-2027·2026-10-28
Medline recalls medical convenience kits due to removal difficulty and skin residue
Medline Industries is recalling 146,971 medical convenience kits because they are difficult to remove from patients and leave adhesive residue on the skin.
Product
MEDLINE medical convenience kits labeled as: (list truncated)
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0235-2027·2026-10-28
Boston Scientific Recalls Defective Direxion Torqueable Microcatheters
Boston Scientific is recalling 632 Direxion Torqueable Microcatheters due to insufficient UV curing of the hydrophilic coating and raised ridges on nitinol sleeves.
Product
Direxion Torqueable Microcatheter, NGMC/SINGLE/021/STRAIGHT/2RO/130; Material Number: M001195320
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0281-2027·2026-10-28
Medline Recalls Hip Scope Packs Due to Removal Difficulties
Medline Industries is recalling 56 hip scope packs because they are difficult to remove and leave adhesive residue on patient skin.
Product
MEDLINE medical convenience kits labeled as: 1) HIP SCOPE PACK, Medline Kit Number/SKU DYNJ64103C; 2) HIP SCOPE PACK, Medline Kit Number/SKU DYNJ64155B.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0076-2027·2026-10-28
Hikma Recalls Abirtega Tablets for Weight Uniformity Failures
Hikma Pharmaceuticals is recalling Abirtega (abiraterone acetate) 250 mg tablets because they failed weight uniformity specifications.
Product
ABIRTEGA — ABIRTEGA (ABIRATERONE ACETATE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0271-2027·2026-10-28
Medline C-Section Drapes Recalled for Adhesive Removal Issues
Medline Industries is recalling C-section drapes that are difficult to remove and leave adhesive residue on patient skin.
Product
MEDLINE DRAPE C-SECTION FEN CLR SCREEN W, Medline Product Number/SKU DYNJP6108
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0240-2027·2026-10-28
Boston Scientific Recalls Direxion Torqueable Microcatheters for Coating Defects
Boston Scientific is recalling 902 Direxion Torqueable Microcatheters due to insufficient UV curing of the hydrophilic coating and raised ridges on nitinol sleeves.
Product
Direxion Torqueable Microcatheter, NGMC/SINGLE/027/STRAIGHT/1RO/130; Material Number: M001195410
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Food)·H-0119-2027·2026-10-28
El Ruisenor De Mexico Recalls Soybeans for Undeclared Soy Allergen
El Ruisenor De Mexico, Inc. is recalling soybeans in clear plastic packages because they contain an undeclared soy allergen. The product was distributed primarily to California and limited customers in other states.
Product
Soybeans; packed in a clear plastic 1lb, 5lb, 50lb unit sizes. No UPC
Category
Food
Distribution
7 states
ModerateFDA (Drugs)·D-0054-2027·2026-10-28
Pritam International Recalls Brush Buddies Fluoride Toothpaste for CGMP Deviations
Pritam International is voluntarily recalling 411,600 tubes of Brush Buddies Hot Wheels Anticavity Fluoride Toothpaste due to Current Good Manufacturing Practice (CGMP) deviations.
Product
Brush Buddies, Hot Wheels, Anticavity Fluoride Toothpaste, (sodium fluoride 0.243%) Strawberry Flavor, Net Wt. 4.0 oz (113g), Distributed by Ashtel Studios Inc., Ontario, California 91761, NDC 84140-002-40, Item # 88047, UPC 8 10147 88047 8
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0194-2027·2026-10-28
Medtronic NDI Passive Spheres Recalled for Reflective Material Variation
Medtronic is recalling NDI Passive Spheres and biopsy needle kits because reflective material variation may affect the navigation system's ability to detect and track the spheres.
Product
Medtronic NDI Passive Spheres REF: 8801071, Sterile EO, 1/Tray 12 pk., Rxonly
Category
Medical Device
Distribution
52 states
ModerateFDA (Food)·H-0163-2027·2026-10-28
El Ruisenor De Mexico Recalls Wheat Germ for Undeclared Wheat Allergen
El Ruisenor De Mexico, Inc. is recalling 11 pounds of wheat germ packaged in clear plastic units due to an undeclared wheat allergen. The product was distributed primarily to California customers.
Product
Wheat Germ; packaged in 1lb, 5lb, 50lb clear plastic units. No UPC
Category
Food
Distribution
7 states
ModerateFDA (Food)·H-0144-2027·2026-10-28
El Ruisenor De Mexico Recalls Walnut Halves for Undeclared Allergen
El Ruisenor De Mexico, Inc. is recalling walnut halves due to an undeclared allergen ingredient. The product was distributed primarily in California and limited to other states.
Product
Walnut halves; packaged in 1lb, 5lb, 22-25lb clear plastic units. No UPC
Category
Food
Distribution
7 states
ModerateFDA (Food)·H-0160-2027·2026-10-28
El Ruisenor De Mexico Recalls Wheat Snacks for Undeclared Wheat
El Ruisenor De Mexico, Inc. is recalling 4X6 and 4X8 Wheat Snacks because they contain an undeclared wheat allergen.
Product
4X6 Wheat Snack; packaged in 1lb, 5lb, 33lb clear plastic units. 4X8 Wheat Snack; packaged in 1lb, 5lb, 33lb clear plastic units. No UPC
Category
Food
Distribution
7 states
ModerateFDA (Devices)·Z-0233-2027·2026-10-28
Boston Scientific Recalls Direxion Torqueable Microcatheters for Coating Defects
Boston Scientific is recalling 3,284 Direxion Torqueable Microcatheters due to insufficient UV curing of the hydrophilic coating and raised ridges on nitinol sleeves.
Product
Direxion Torqueable Microcatheter, NGMC/SINGLE/021/SWAN/1RO/130; Material Number: M001195300
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Food)·H-0152-2027·2026-10-28
El Ruisenor De Mexico Recalls Shelled White Pine Nuts for Undeclared Allergen
El Ruisenor De Mexico, Inc. is recalling shelled white pine nuts due to an undeclared allergen ingredient. The product was distributed primarily in California and limited to other states.
Product
Shelled White Pine Nuts; packaged in 1lb, 5lb, 25-55lb clear plastic units. No UPC
Category
Food
Distribution
7 states
ModerateFDA (Drugs)·D-0066-2027·2026-10-28
Brush Buddies Toothpaste Recalled for Manufacturing Deviations
Pritam International is voluntarily recalling Brush Buddies toothpaste nationwide due to CGMP deviations. No illnesses or injuries are reported.
Product
BB (Brush Buddies) Cavity Protection, Anti-Cavity Fluoride Toothpaste, (sodium monofluorophosphate 0.76%) Cool Mint, 2 Value Pack, Two 3.5 oz (99g) tubes, Total Net Wt 7 oz (198g), Distributed by Ashtel Studios Inc., Ontario, California 91761, NDC 84140-035-10, Item # 88543, UPC…
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0067-2027·2026-10-28
Pritam International Recalls Brush Buddies Toothpaste Due to CGMP Deviations
Pritam International is voluntarily recalling 198,288 tubes of Brush Buddies toothpaste nationwide due to Current Good Manufacturing Practice (CGMP) deviations.
Product
BB (Brush Buddies) Advanced Whitening, Anti-Cavity Fluoride Toothpaste, (sodium fluoride 0,24%) Peppermint, Net Wt 3.5 oz (99g), Distributed by Ashtel Studios Inc., Ontario, California 91761, NDC 84140-885-42, Item # 88542, UPC 8 10147 88542 8
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Food)·H-0105-2027·2026-10-28
El Ruisenor De Mexico Recalls Hulled Sesame Seeds for Undeclared Allergen
El Ruisenor De Mexico, Inc. is recalling hulled sesame seeds due to an undeclared sesame allergen. The product was distributed primarily in California and limited areas in six other states.
Product
Hulled Sesame Seeds; packed in a clear plastic bag. 1lb, 5lb, 50lb unit size. No UPC
Category
Food
Distribution
7 states
ModerateFDA (Devices)·Z-0276-2027·2026-10-28
Medline Medical Convenience Kits Recalled for Adhesive Removal Issues
Medline Industries is recalling 2,229 medical convenience kits because they are difficult to remove from patients and leave adhesive residue on the skin.
Product
MEDLINE medical convenience kits labeled as: 1) BIRTHDAY KIT-DOUBLE BASIN-LF, Medline Kit Number/SKU DYNJ16127N; 2) NYGH-DELIVERY PACK-LF, Medline Kit Number/SKU DYNJ27206D; 3) OB/GYN, Medline Kit Number/SKU DYNJ911652.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0231-2027·2026-10-28
Boston Scientific Recalls Direxion Torqueable Microcatheters for Coating Defects
Boston Scientific is recalling 381 units of Direxion Torqueable Microcatheters due to insufficient UV curing of the hydrophilic coating and raised ridges on nitinol sleeves.
Product
Direxion Torqueable Microcatheter, NGMC/SINGLE/021/J/1RO/155; Material Number: M001195280
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0193-2027·2026-10-28
B Braun SAFSITE Injection Site Valve Recall for Leakage Risk
B Braun Medical Inc is recalling SAFSITE Injection Site valves due to a potential for leakage and backflow.
Product
B Braun SAFSITE Injection Site, RV1000NC SAFSITE VALVE W/O EXTRA CAP. Catalog Number: 415068.
Category
Medical Device
Distribution
Distributed nationwide

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126–150 of 114834