Florida recalls
4323 federal recalls on file affecting Florida - 944 Florida-specific plus 3379 nationwide. Sourced from CPSC, FDA, USDA, and NHTSA.
- 2026-02-11FDA-FoodImu-Tek Animal HealthClass IIStop using Imu-Tek Immuno-5 Colostrum Powder
Undeclared milk allergen
- 2026-02-11FDA-FoodDiva FamClass IINationwideStop using Diva Fam Sea Moss Gel Superfood
potential Clostridium botulinum contamination
- 2026-02-11FDA-FoodDiva FamClass IINationwideStop using Diva Fam Sea Moss Gel Superfood
potential Clostridium botulinum contamination
- 2026-02-11FDA-FoodDiva FamClass IINationwideStop using Diva Fam Sea Moss Gel Superfood
potential Clostridium botulinum contamination
- 2026-02-11FDA-FoodDiva FamClass IINationwideStop using Diva Fam Sea Moss Gel Superfood
potential Clostridium botulinum contamination
- 2026-02-11FDA-FoodDiva FamClass IINationwideStop using Diva Fam Sea Moss Gel Superfood
potential Clostridium botulinum contamination
- 2026-02-11FDA-FoodDiva FamClass IINationwideStop using Diva Fam Sea Moss Gel Superfood
potential Clostridium botulinum contamination
- 2026-02-11FDA-FoodDiva FamClass IINationwideStop using Diva Fam strawberry sea moss gel
potential Clostridium botulinum contamination
- 2026-02-11FDA-FoodDiva FamClass IINationwideStop using Diva Fam Sea Moss Gel Superfood
potential Clostridium botulinum contamination
- 2026-02-11FDA-FoodDiva FamClass IINationwideStop using Diva Fam Sea Moss Gel Superfood
potential Clostridium botulinum contamination
- 2026-02-11FDA-FoodDiva FamClass IINationwideStop using Diva Fam Sea Moss Gel Superfood
potential Clostridium botulinum contamination
- 2026-02-11FDA-FoodDiva FamClass IINationwideStop using Diva Fam Sea Moss Gel Superfood
potential Clostridium botulinum contamination
- 2026-02-11FDA-FoodDiva FamClass IINationwideStop using Diva Fam sea moss gel
potential Clostridium botulinum contamination
- 2026-02-11FDA-FoodDiva FamClass IINationwideStop using Diva Fam Sea Moss Gel Superfood
potential Clostridium botulinum contamination
- 2026-02-11FDA-FoodDiva FamClass IINationwideStop using Diva Fam mango sea moss gel
potential Clostridium botulinum contamination
- 2026-02-11FDA-FoodBeacon PromotionsClass IIRepackaged M&Ms candies, Net Wt 1.3 oz. Item BB458BG. Labeled with the following promotional company names. 1. Next Up, 2. Smith Pro, 3. Jaxport, Jacksonville Port Authority, 4. Climax Molybdenum, A Freeport-McMoRan Company, 5. University of Maryland, School of Public Policy, 6. Liberty University Environmental Health & Safety, 7. Subaru, 8. Trinity Cyb3r, 9. Candy Treats, 10. JSE, Jordan & Skala Engineers, 11. Dropbox DocSend, 12. PP, Prosperity Promotions, 1
Undeclared allergens (milk, soy, and peanut)
- 2026-02-11FDA-FoodBeacon PromotionsClass IIStop eating Make Your Mark M&Ms candy
Undeclared allergens (milk, soy, and peanut)
- 2026-02-11FDA-FoodTai Phat WholesalersClass IStop using Sofit Seedless Red Dates
Undeclared sulfites
- 2026-02-11FDA-FoodPrima FoodsClass IIIStop using BarbaCuban Havana Gold
Undeclared Quinine
- 2026-02-11FDA-FoodPrima FoodsClass IIIStop using BarbaCuban Cubama White Truffle Sauce
Undeclared Quinine
- 2026-02-11FDA-FoodPrima FoodsClass IIIStop using BarbaCuban Ram Air Red Zesty Ketchup
Undeclared Quinine
- 2026-02-11FDA-FoodPrima FoodsClass IIIStop using BarbaCuban 455 Everything Sauce
Undeclared Quinine
- 2026-02-11FDA-FoodPrima FoodsClass IIIStop using BarbaCuban 90 Miles to Mojo Marinade
Undeclared Quinine
- 2026-02-11FDA-FoodPrima FoodsClass IIIStop using BarbaCuban 455 Everything Sauce
Undeclared Quinine
- 2026-02-11FDA-FoodOptiwizeClass IIINationwideStop using OptiWize Collagen Plus
The firm initiated a voluntary recall after NSF testing showed that labeled ingredient quantities did not align with analytical test results, manganese level was below label quantity.
- 2026-02-11FDA-FoodFazt & LoudClass IIINationwideStop drinking Fazt & Loud Lost and Found Energy
Recall is due to a misprint on the label that incorrectly identifies the total caffeine content on the can. The item contains 300mg of caffeine, instead of 150mg as provided on the can.
- 2026-02-11FDA-DrugSun PharmaceuticalClass IINationwideStop using Sun Pharmaceutical Diclofenac Sodium Gel
Failed Viscosity Specifications: Out of Specification (OOS) [slightly lower than the limit] result in viscosity for Diclofenac Sodium Gel, 3%.
- 2026-02-11FDA-DrugGranulesClass IINationwideStop using Granules trazodone 50 mg
Presence of Foreign Tablets/Capsules
- 2026-02-11FDA-DrugGreen LumberClass INationwideStop using Green Lumber Natural Fuel For Men
Marketed without an Approved NDA/ANDA: FDA analysis found this product to contain tadalafil
- 2026-02-11FDA-DrugUnichem PharmaceuticalsClass IINationwideStop using Unichem bisoprolol/hydrochlorothiazide tablets
cGMP Deviations: recall due to not meeting the N-Nitroso Bisoprolol impurity specification limits.
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