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. 2,622 recalls have been distributed to Florida in the last 12 months.
Showing 44041–44060 of 55,837 recalls
Recalled Item: MediChoice WarmGel Infant Heel Warmer Recalled by CooperSurgical, Inc. Due...
The Issue: Products without expiration date have the remote potential for minor burn
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CooperSurgical Infant Heel Gel Warmers Recalled by CooperSurgical, Inc. Due...
The Issue: Products without expiration date have the remote potential for minor burn
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fisher Brand Gel Infant Heel Gel Warmers Recalled by CooperSurgical, Inc....
The Issue: Products without expiration date have the remote potential for minor burn
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NovaPlus Brand Warm Gel Infant Heel Gel Warmer Recalled by CooperSurgical,...
The Issue: Products without expiration date have the remote potential for minor burn
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EDGE Amplified Weight Release capsules Recalled by Detox Transforms Due to...
The Issue: Marketed Without An Approved NDA/ANDA: Product was found to contain...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: BtRiM Max capsules Recalled by Detox Transforms Due to Undeclared...
The Issue: Marketed Without An Approved NDA/ANDA: Product was found to contain...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: iNDiGO capsules Recalled by Detox Transforms Due to Undeclared Phenolphthalein
The Issue: Marketed Without An Approved NDA/ANDA: Product was found to contain...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: AMPD GOLD Bee Pollen capsules Recalled by Detox Transforms Due to Undeclared...
The Issue: Marketed Without An Approved NDA/ANDA: Product was found to contain...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: iNSANE Bee Pollen capsules Recalled by Detox Transforms Due to Undeclared...
The Issue: Marketed Without An Approved NDA/ANDA: Product was found to contain...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: CHILI POWDER 50 LBS Recalled by Wm. E. Martin & Sons Co., Inc. Due to...
The Issue: Cumin contains undeclared peanut protein
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: GROUND CUMIN STERILE TREATED PROD. OF TURKEY Recalled by Wm. E. Martin &...
The Issue: Cumin contains undeclared peanut protein
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: KETOROLAC Tromethamine Inj. Recalled by Hospira Inc. Due to Crystallization
The Issue: Crystallization
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: KETOROLAC Tromethamine Inj. Recalled by Hospira Inc. Due to Crystallization
The Issue: Crystallization
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Nicardipine Hydrochloride Injection Recalled by Mylan Institutional LLC Due...
The Issue: Subpotent Drug and Failed Impurities/Degradation Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: PROBAR Frosted Peanut Butter BASE Protein Bar Recalled by Probar LLC Due to...
The Issue: PROBAR, LLC has initiated a voluntary recall of its PROBAR Base Frosted...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Bio-MAC Cannula (Needle) Set Recalled by Biologic Therapies, Inc Due to...
The Issue: Devices are misbranded - failure to properly classify and obtain FDA...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bio-CORE Cannula (Needle) Set Recalled by Biologic Therapies, Inc Due to...
The Issue: Devices are misbranded - failure to properly classify and obtain FDA...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bio-PLASTY Cannula (Needle) Recalled by Biologic Therapies, Inc Due to...
The Issue: Devices are misbranded - failure to properly classify and obtain FDA...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Passport V Monitor Recalled by Mindray DS USA, Inc. dba Mindray North...
The Issue: An issue has been identified with Passport V Monitors invasive blood...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MAX-TL 9.0 x 7.0 mm Implant Recalled by Southern Implants, Inc Due to Z-MAX...
The Issue: Z-MAX Implant, 9mm diameter, 7mm length labeled package, catalog number...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.