Product Recalls in Florida
Product recalls affecting Florida — including food, drugs, consumer products, medical devices, and vehicles distributed to Florida. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,866 recalls have been distributed to Florida in the last 12 months.
Showing 12821–12840 of 55,837 recalls
Recalled Item: Esomeprazole Magnesium Delayed-Release Capsules Recalled by SUN...
The Issue: Superpotent Drug: Out of specification for assay at the 12-month timepoint.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Esomeprazole Magnesium Delayed-Release Capsules Recalled by SUN...
The Issue: Superpotent Drug: Out of specification for assay at the 12-month timepoint.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Testosterone Cypionate Injection Recalled by SUN PHARMACEUTICAL INDUSTRIES...
The Issue: cGMP - Water leakage
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: SoDelicious DairyFree Wondermilk Dairy Free Frozen Dessert Salted Caramel...
The Issue: A small number of individual cones with peanut pieces were mistakenly packed...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: AquaC UNO H [120V Recalled by Fresenius Medical Care Holdings, Inc. Due to...
The Issue: Internal ethemet cables are missing one or both ferrite cores therefore the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AquaC UNO H [120V Recalled by Fresenius Medical Care Holdings, Inc. Due to...
The Issue: Internal ethemet cables are missing one or both ferrite cores therefore the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: etouchus Recalled by Touch US Llc Due to Device was marketed without FDA...
The Issue: Device was marketed without FDA 510(k) clearance or a PMA.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Description/Part: Simplify Disc Size 1 Recalled by NuVasive Inc Due to...
The Issue: Cervical artificial disc Unique Device Identifier (UDI) barcodes contain the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Intraosseous needle and driver. Catalog/Device Name: D015151NK/BD Needle Kit...
The Issue: BD Intraosseous Needle Kits may exhibit: 1) Increased force required to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Daily Harvest French Lentil + leek Crumbles Recalled by DAILY HARVEST Due to...
The Issue: Product is linked to complaints of gastrointestinal illness.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Verigene CDF Nucleic Acid Test Recalled by Luminex Corporation Due to There...
The Issue: There is a potential for false negative results using VERIGENE CDF Stool...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Merlin 2 PCS MER37000 programmer Model MER3400 software Recalled by St. Jude...
The Issue: The Merlin" 2 PCS model MER3700 is a portable, dedicated programming system...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Merlin PCS 3650 programmer Model 3330 software Recalled by St. Jude Medical,...
The Issue: There is a potential for programmer software (Merlin PCS) and remote...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Merlin.net model MN5000 Software Recalled by St. Jude Medical, Cardiac...
The Issue: The Merlin" 2 PCS model MER3700 is a portable, dedicated programming system...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VERIGENE Enteric Pathogens Nucleic Acid Test Recalled by Luminex Corporation...
The Issue: There is a potential for false negative results using VERIGENE CDF Stool...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Draximage MAA (Kit for the preparation of Technnetium Tc 99m Recalled by...
The Issue: Lack of Assurance of Sterility: Out-of-specification test results obtained...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Eszopiclone Tablets Recalled by Macleods Pharma Usa Inc Due to Shortfill:...
The Issue: Shortfill: customer complaints of one to three tablets were reported missing...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Mometasone Furoate Recalled by Glenmark Pharmaceuticals Inc., USA Due to...
The Issue: Defective Container
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Various ob/gyn packs Recalled by American Contract Systems, Inc. Due to...
The Issue: Product was exposed to multiple sterilization cycles without validation for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Various Angiography packs/trays Recalled by American Contract Systems, Inc....
The Issue: Product was exposed to multiple sterilization cycles without validation for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.