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

5051–5075 of 90255

CriticalFDA (Food)·H-0171-2026·2025-11-12
Repackaged shell eggs recalled over potential Salmonella contamination in retail brands
Eggs Unlimited is recalling 92,476 units of shell eggs sold under Big Y, Simple Truth, Stater Bros, That's Smart, Lindsey's Gold and Marketside labels over potential Salmonella.
Product
Big Y Brown Jumbo A 12ct Eggs; UPC: 018894319146 Simple Truth Cage Free Brown Large AA 12ct; UPC: 011110797698 Stater Bros Cage Free Large AA 18ct; 074175001650 That's Smart Cage Free Large AA 60ct; 193476006192 Lindsey s Gold Free Range Brown Large A 12ct; 860011334408…
Category
Food
Distribution
3 states
CriticalFDA (Food)·H-0153-2026·2025-11-12
Farm shell eggs recalled over potential Salmonella contamination in New York
Jacob King is recalling approximately 15 dozen in-shell chicken eggs distributed from a farm in Addison, New York, over potential Salmonella. The FDA has classified it Class I.
Product
In-shell chicken eggs distributed on Jacob King's farm in Addison, NY
Category
Food
Distribution
1 state
CriticalFDA (Devices)·Z-0374-2026·2025-11-12
Cranial perforators recalled as inadequate weld recall expands to smaller sizes
Integra LifeSciences is recalling 5,109 CODMAN Disposable Perforators, 9mm, extending an existing 14 mm recall for inadequate welds. The FDA has classified it Class I.
Product
CODMAN Disposable Perforator 9mm. Cranial Perforator.
Category
Medical Device
Distribution
Distributed nationwide
CriticalFDA (Devices)·Z-0373-2026·2025-11-12
Eleven millimetre cranial perforators recalled over inadequate welds
Integra LifeSciences is recalling 16,251 CODMAN Disposable Perforators, 11mm, extending an existing 14 mm recall for inadequate welds. The FDA has classified it Class I.
Product
CODMAN Disposable Perforator 11mm. Cranial Perforator.
Category
Medical Device
Distribution
Distributed nationwide
CriticalFDA (Food)·H-0156-2026·2025-11-12
Soft taco dinner kits recalled over an undeclared milk allergen
Teasdale Foods is recalling 3,654 cases, 21,924 units, of Casa Mamita Soft Taco Dinner Kit sold at ALDI over undeclared milk. The FDA has classified the recall as Class I.
Product
Casa Mamita Soft Taco Dinner Kit, Net Wt 13.4 OZ (379g), UPC: 4099100318715, DIST. & SOLD EXCLUSIVELY BY: ALDI BATAVIA, IL 60510 Product consists of 10 flour tortillas, 1 sauce packet, and 1 seasoning packet within a carton; 6 cartons are packed into a mixed case with 6…
Category
Food
Distribution
11 states
CriticalFDA (Devices)·Z-0427-2026·2025-11-12
Insulin pumps recalled over false vibration motor failure stopping delivery
Tandem Diabetes Care is recalling 17,745 Tandem Mobi insulin pumps because a software issue can trigger a false vibration motor failure that halts insulin delivery. The FDA classified it Class I.
Product
Tandem Mobi Insulin Pump: Description/Catalog: Tandem insulin pumps are battery-operated infusion pumps capable of both basal and bolus delivery of insulin. The pumps utilize a motor-driven mechanism to deliver insulin from within a disposable cartridge, through an infusion…
Category
Medical Device
Distribution
53 states
SevereNHTSA·25V778000·2025-11-12
Yamaha Recalls 2018-2022 XMAX Scooters Due to Camshaft Bolt Issue
Yamaha is recalling 2,715 XMAX scooters because a camshaft bolt may loosen, causing engine stalls and increasing crash risk.
Product
YAMAHA — YAMAHA XMAX
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·25V777000·2025-11-12
Audi SUVs recalled because seat belt buckles may be missing a rivet
Volkswagen Group of America is recalling certain 2025 Audi Q7, Q8, SQ8 and RS Q8 vehicles because the front seat belt buckles may be missing a rivet that secures the buckle to the stalk.
Product
AUDI — AUDI Q8, Q7, RS Q8, SQ8
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Food)·H-0161-2026·2025-11-12
Waterfront Bistro shrimp recalled over potential Cesium-137 contamination
AquaStar is recalling 3,600 cases of Waterfront Bistro Frozen Raw EZ-Peel White Shrimp 21/25 because the shrimp may be contaminated with Cesium-137.
Product
Waterfront Bistro Frozen Raw EZ-Peel White Shrimp 21/25, net wt. 2lbs., UPC 021130123223. Product was sold at Shaw s and Star Market, Albertson's, Eagle, Carrs-Safeway, and Safeway.
Category
Food
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0151-2026·2025-11-12
Amoxicillin clavulanate oral suspension recalled as subpotent in the clavulanate component
Teva Pharmaceuticals USA is recalling 4,680 cartons of Amoxicillin and Clavulanate Potassium for Oral Suspension 200 mg/28.5 mg per 5 mL because the clavulanate component is subpotent.
Product
Amoxicillin and Clavulanate Potassium for Oral Suspension USP, 200 mg/28.5 mg per 5mL, 100 mL (when reconstituted), Rx only, manufactured in Canada by: Teva Canada Limited, Toronto, Canada M1B 2K9; Manufactured For: Teva Pharmaceuticals USA, Inc., Parsippany, NJ 07054 NDC…
Category
Drug
Distribution
3 states
HighFDA (Drugs)·D-0155-2026·2025-11-12
Pain relief caplets recalled because the box names the wrong drug
Aero Healthcare is recalling two lots of AERO TAB caplets because the outer box states acetaminophen and caffeine while the inner pouch correctly states aspirin and caffeine.
Product
AEROTAB PAIN RELIEVER — AEROTAB PAIN RELIEVER (PAIN RELIEVER)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Food)·H-0151-2026·2025-11-12
Veggie burgers recalled after equipment tested positive for Listeria
Dr. Praeger's Sensible Foods is recalling 648 master cases of California Veggie Burgers because the product was made on equipment that tested positive for Listeria.
Product
Dr. Praeger's, California Veggie Burgers, 10oz, Plastic wrapped burgers inside of a retail box. 6 packages per master case. Keep Frozen
Category
Food
Distribution
3 states
HighFDA (Drugs)·D-0152-2026·2025-11-12
Clomipramine 25 mg capsules recalled over nitrosamine above the intake limit
Zydus Pharmaceuticals is recalling clomiPRAMINE Hydrochloride Capsules USP 25 mg after N-Nitroso Desmethyl-Clomipramine was found above the FDA acceptable intake limit.
Product
CLOMIPRAMINE HYDROCHLORIDE — CLOMIPRAMINE HYDROCHLORIDE (CLOMIPRAMINE HYDROCHLORIDE)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0153-2026·2025-11-12
Clomipramine 50 mg capsules recalled over nitrosamine above the intake limit
Zydus Pharmaceuticals is recalling clomiPRAMINE Hydrochloride Capsules USP 50 mg after N-Nitroso Desmethyl-Clomipramine was found above the FDA acceptable intake limit.
Product
CLOMIPRAMINE HYDROCHLORIDE — CLOMIPRAMINE HYDROCHLORIDE (CLOMIPRAMINE HYDROCHLORIDE)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Food)·H-0154-2026·2025-11-12
Ground ginger recalled over elevated levels of lead in one lot
Eagle Spice and Extract is recalling 2,476 units of Eagle Spice Ground Ginger 16 oz because the product contains elevated levels of lead.
Product
Eagle Spice Ground Ginger 16 oz.
Category
Food
Distribution
4 states
HighFDA (Food)·H-0152-2026·2025-11-12
Frozen coconut bars recalled over sulfites undeclared on the product label
Que Rikura's Products is recalling 31,953 cases of 4 oz frozen coconut bars distributed in Florida because sulfites are undeclared on the product label.
Product
Frozen Coconut bar Net wt. 4oz (113g) single bars packed in a plastic cup. UPC: 61058590845. Crafted by Fruitique International Miami USA 33016. Phone 1(888)960-6024
Category
Food
Distribution
1 state
HighFDA (Devices)·Z-0423-2026·2025-11-12
Curved extension catheter trays 20 cm recalled over header bag seals
Mozarc Medical is recalling 3,258 MAHURKAR acute high pressure triple lumen catheter trays with curved extensions, 12 Fr x 20 cm, over header bag seal integrity.
Product
MAHURKAR" Acute High Pressure Triple Lumen Catheter Tray Curved Extensions with IC Components: 12 Fr/Ch (4.0 mm) x 20 cm;
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·25V776000·2025-11-12
Winnebago Recalls 2025-2026 Micro Minnie Travel Trailers Due to Fire Risk
Winnebago is recalling 2025-2026 Micro Minnie travel trailers because the cooktop flame may invert when the stove and furnace operate simultaneously, increasing fire risk.
Product
WINNEBAGO — WINNEBAGO MICRO MINNIE
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Food)·H-0166-2026·2025-11-12
Strawberry cheesecake ice cream recalled over foil fragments in brown sugar
Ice Cream Factory is recalling 979 cases and 313 tubs of Strawberry Cheesecake ice cream after aluminum foil and packaging fragments were found in a brown sugar ingredient.
Product
Strawberry Cheesecake Ice Cream with graham crackers swirl, 12 oz pack, Single Cup Net Wt: 8.75oz, Case of 12 Strawberry Cheesecake with graham cracker swirl, 2.5-gal Tub, Net Weight 14 pounds Labels read in part as "Ice Cream Factory, Distributed by Ice Cream Factory 1201 Ice…
Category
Food
Distribution
29 states
HighFDA (Drugs)·D-0154-2026·2025-11-12
Clomipramine 75 mg capsules recalled over nitrosamine above the intake limit
Zydus Pharmaceuticals is recalling clomiPRAMINE Hydrochloride Capsules USP 75 mg after N-Nitroso Desmethyl-Clomipramine was found above the FDA acceptable intake limit.
Product
CLOMIPRAMINE HYDROCHLORIDE — CLOMIPRAMINE HYDROCHLORIDE (CLOMIPRAMINE HYDROCHLORIDE)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0419-2026·2025-11-12
Size G hip bearings recalled over commingled implant sizes in packaging
Zimmer is recalling 63 Dual Mobility Vivacit-E bearings labelled Size G 46 mm because the package contents and label may be commingled with the Size F 44 mm bearing.
Product
Zimmer Biomet Dual Mobility Vivacit-E Highly Crosslinked Polyethylene, 28 mm I.D., 46 mm O.D., Size G, Bearing, Model/Catalog Number: 110031013; semi constrained hip prosthesis
Category
Medical Device
Distribution
20 states
HighFDA (Food)·H-0164-2026·2025-11-12
Extra large peeled shrimp recalled over potential Cesium-137 contamination
AquaStar is recalling 1,458 cases of Publix Extra Large Shrimp Easy to Peel Deveined 21/25 because the shrimp may be contaminated with Cesium-137.
Product
Publix Extra Large Shrimp Easy to Peel Deveined 21/25, net wt. 1.5 lbs. UPC 041415064454. Product was sold at Publix.
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0429-2026·2025-11-12
Chemistry analyzers recalled over gantry defect that pauses the instrument
Beckman Coulter is recalling 657 UniCel DxI 800 analyzers because defective gantry sub-components can cause a z-axis motion error that halts the analyzer and delays results.
Product
Beckman Coulter UniCel DxI 800, Part Numbers: 973100, A71456; Photometric Chemistry Analyzer
Category
Medical Device
Distribution
0 states
HighFDA (Devices)·Z-0422-2026·2025-11-12
Dialysis catheter trays recalled over seal integrity of header bag packaging
Mozarc Medical is recalling 3,258 MAHURKAR acute high pressure triple lumen catheter trays, 12 Fr x 16 cm, over a potential issue with the seal integrity of the header bag packaging.
Product
MAHURKAR" Acute High Pressure Triple Lumen Catheter Tray Curved Extensions with IC Components: 12 Fr/Ch (4.0 mm) x 16 cm;
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0421-2026·2025-11-12
Curved extension catheter trays recalled over header bag seal integrity
Mozarc Medical is recalling 3,258 MAHURKAR acute high pressure triple lumen catheter trays, 12 Fr x 13 cm, over a potential issue with the seal integrity of the header bag packaging.
Product
MAHURKAR" Acute High Pressure Triple Lumen Catheter Tray Curved Extensions with IC Components: 12 Fr/Ch (4.0 mm) x 13 cm;
Category
Medical Device
Distribution
Distributed nationwide

How to read this listing

Filters

5051–5075 of 90255