FoodFeb 11, 2026
Diva Fam Sea Moss Gel Superfood recall — FDA H-0479-2026
potential Clostridium botulinum contamination
Class IIFDA: TerminatedDiva Fam Inc
Monthly breakdown
2026 recalls by month
Select a month to review the recall records reported during that period.
August 2026145 records · 4 categoriesJuly 2026369 records · 4 categoriesJune 2026373 records · 4 categoriesMay 2026332 records · 4 categoriesApril 2026407 records · 4 categoriesMarch 2026179 records · 4 categoriesFebruary 2026329 records · 4 categoriesJanuary 2026210 records · 4 categories
2026 recalls — page 86
Records are ordered by the best available source date.
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.
About the 2026 recall archive
This archive groups records by their reported or recall date. It does not imply that every recall was initiated, announced and resolved during the same calendar year. Open the individual record for the exact dates and source details supplied by FDA or NHTSA.