Latest U.S. Recalls — FDA & NHTSA Records

Latest records

Latest recalls — page 86

The newest recall records with useful source details are listed here.

FoodFeb 11, 2026

Diva Fam Sea Moss Gel Superfood recall — FDA H-0479-2026

potential Clostridium botulinum contamination

Class IIFDA: TerminatedDiva Fam Inc

FoodFeb 11, 2026

Prima Foods International BarbaCuban Ram Air Red Zesty Ketchup, Net Wt recall — FDA H-0446-2026

Undeclared Quinine

Class IIIFDA: TerminatedPrima Foods International, Inc.

FoodFeb 11, 2026

Prima Foods International BarbaCuban Cubama White Truffle Sauce, Net Wt recall — FDA H-0447-2026

Undeclared Quinine

Class IIIFDA: TerminatedPrima Foods International, Inc.

FoodFeb 11, 2026

Diva Fam Sea Moss Gel Superfood recall — FDA H-0471-2026

potential Clostridium botulinum contamination

Class IIFDA: TerminatedDiva Fam Inc

FoodFeb 11, 2026

Diva Fam Sea Moss Gel Superfood recall — FDA H-0475-2026

potential Clostridium botulinum contamination

Class IIFDA: TerminatedDiva Fam Inc

FoodFeb 11, 2026

Willy Pete's Chocolates brand Almond Despair recall — FDA H-0484-2026

Almonds are not declared in the ingredient statement. Almond is included in description of product on front label.

Class IIIFDA: TerminatedWilly Pete's Chocolate Company LLC

FoodFeb 11, 2026

Prima Foods International BarbaCuban 455 Everything Sauce recall — FDA H-0443-2026

Undeclared Quinine

Class IIIFDA: TerminatedPrima Foods International, Inc.

FoodFeb 11, 2026

Diva Fam Sea Moss Gel Superfood recall — FDA H-0468-2026

potential Clostridium botulinum contamination

Class IIFDA: TerminatedDiva Fam Inc

FoodFeb 11, 2026

Diva Fam Sea Moss Gel Superfood recall — FDA H-0480-2026

potential Clostridium botulinum contamination

Class IIFDA: TerminatedDiva Fam Inc

FoodFeb 11, 2026

Khee Trading Product is Frozen Half Shell Oysters in 15-16 pound blocks recall — FDA H-0482-2026

Imported oysters potentially contaminated with Norovirus

Class IIFDA: TerminatedKhee Trading, Inc.

FoodFeb 11, 2026

Diva Fam Sea Moss Gel Superfood recall — FDA H-0477-2026

potential Clostridium botulinum contamination

Class IIFDA: TerminatedDiva Fam Inc

FoodFeb 11, 2026

Imu-Tek Immuno-5 Colostrum Powder 7 oz recall — FDA H-0483-2026

Undeclared milk allergen

Class IIFDA: TerminatedImu-Tek Animal Health, Incorporated

FoodFeb 11, 2026

Diva Fam Sea Moss Gel Superfood recall — FDA H-0467-2026

potential Clostridium botulinum contamination

Class IIFDA: TerminatedDiva Fam Inc

FoodFeb 11, 2026

VH FOODS Bread Crumbs, Outside The Breadbox brand, net wt recall — FDA H-0481-2026

Undeclared allergens: egg and milk

Class IFDA: TerminatedVH FOODS INC

FoodFeb 11, 2026

Diva Fam Sea Moss Gel Superfood recall — FDA H-0478-2026

potential Clostridium botulinum contamination

Class IIFDA: TerminatedDiva Fam Inc

FoodFeb 11, 2026

Diva Fam Sea Moss Gel Superfood recall — FDA H-0469-2026

potential Clostridium botulinum contamination

Class IIFDA: TerminatedDiva Fam Inc

FoodFeb 11, 2026

Beacon Promotions Repackaged M&Ms candies, Net Wt 1.3 oz recall — FDA H-0462-2026

Undeclared allergens (milk, soy, and peanut)

Class IIFDA: OngoingBeacon Promotions Inc

FoodFeb 11, 2026

Diva Fam Sea Moss Gel Superfood recall — FDA H-0472-2026

potential Clostridium botulinum contamination

Class IIFDA: TerminatedDiva Fam Inc

DrugFeb 11, 2026

Diclofenac Sodium, Topical Gel, 3%, 100 g tube recall — FDA D-0342-2026

Failed Viscosity Specifications: Out of Specification (OOS) [slightly lower than the limit] result in viscosity for Diclofenac Sodium Gel, 3%.

Class IIFDA: OngoingSUN PHARMACEUTICAL INDUSTRIES INC

DrugFeb 11, 2026

Green Lumber Natural Fuel For Men capsule recall — FDA D-0304-2026

Marketed without an Approved NDA/ANDA: FDA analysis found this product to contain tadalafil

Class IFDA: OngoingGreen Lumber Holdings, LLC

DrugFeb 11, 2026

Bisoprolol Fumarate and Hydrochlorothiazide tablets, USP, 2.5 mg/6.25 mg, 100-count bottle recall — FDA D-0301-2026

cGMP Deviations: recall due to not meeting the N-Nitroso Bisoprolol impurity specification limits.

Class IIFDA: OngoingUnichem Pharmaceuticals USA Inc.

Medical DeviceFeb 4, 2026

CareFusion 303 BD Alaris" Pump Module model 8100 UDI-DI code: 10885403810046 The BD AlarisTM recall — FDA Z-1217-2026

Due to a number of modules flashed with a date and time associated with the daylight savings time (DST) adjustment that may cause connectivity issue with hospital networks. This issue only…

Class IIFDA: OngoingCareFusion 303, Inc.

Medical DeviceFeb 4, 2026

Medline medical procedure convenience kits labeled as: CIRCUMCISION PACK, Kit SKU DYNJ16826O recall — FDA Z-1198-2026

Medline kits were manufactured and distributed containing MASTISOL liquid adhesive which was recalled due to complaints that the butyrate tubing cracked during actuation of the vials of…

Class IIFDA: OngoingMedline Industries, LP

Medical DeviceFeb 4, 2026

NIPRO Technical Services Conductivity Standard Solution Catalog/Model Numbers: 10001, 10011 recall — FDA Z-1185-2026

due to a defect associated with the conductivity values of the solution used to calibrate meters and result in the reporting of incorrect conductivity values for dialysate.

Class IIFDA: OngoingNIPRO Technical Services, Inc.

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