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. 2,615 recalls have been distributed to Florida in the last 12 months.
Showing 52901–52920 of 55,837 recalls
Recalled Item: Sarns high-flow aortic arch cannula Recalled by Terumo Cardiovascular...
The Issue: Flexible Arterial Cannula and High-Flow Aortic Arch Cannula connectors were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sarns flexible arterial cannula Recalled by Terumo Cardiovascular Systems...
The Issue: Flexible Arterial Cannula and High-Flow Aortic Arch Cannula connectors were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sarns high-flow aortic arch cannula Recalled by Terumo Cardiovascular...
The Issue: Flexible Arterial Cannula and High-Flow Aortic Arch Cannula connectors were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sarns flexible arterial cannula Recalled by Terumo Cardiovascular Systems...
The Issue: Flexible Arterial Cannula and High-Flow Aortic Arch Cannula connectors were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sarns high-flow aortic arch cannula Recalled by Terumo Cardiovascular...
The Issue: Flexible Arterial Cannula and High-Flow Aortic Arch Cannula connectors were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sarns flexible arterial cannula Recalled by Terumo Cardiovascular Systems...
The Issue: Flexible Arterial Cannula and High-Flow Aortic Arch Cannula connectors were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Reumofan Plus Recalled by Reumofan Plus USA Due to Undeclared Active
The Issue: Marketed without an approved NDA/ANDA: Product may contain undeclared active...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: buPROPion Hydrochloride Extended - Release Tablets (XL) 300 mg Recalled by...
The Issue: Failed Dissolution Specifications; 8-hours for the 18-month stability...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: LPS Diaphyseal Sleeves Product Usage: The LPS Diaphyseal Sleeves are...
The Issue: DePuy Orthopaedics is initiating a voluntary recall of the LPS Diaphyseal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LPS Diaphyseal Sleeves Product Usage: The LPS Diaphyseal Sleeves are...
The Issue: DePuy Orthopaedics is initiating a voluntary recall of the LPS Diaphyseal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LPS Diaphyseal Sleeves Product Usage: The LPS Diaphyseal Sleeves are...
The Issue: DePuy Orthopaedics is initiating a voluntary recall of the LPS Diaphyseal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LPS Diaphyseal Sleeves Product Usage: The LPS Diaphyseal Sleeves are...
The Issue: DePuy Orthopaedics is initiating a voluntary recall of the LPS Diaphyseal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mitosol (mitomycin for solution) Recalled by Mobius Therapeutics LLC Due to...
The Issue: Non-Sterility: one or more components of the kit have been found to be...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Animas(R) 2020 Insulin Infusion Pump Product Usage: This product is Recalled...
The Issue: Animas has identified a component issue affecting a small supply of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TUNNELOC ROUND HEAD INTERFERENCE SCREW 8MMX25MM Biomet Sports Medicine...
The Issue: Thru hole at the tip of the screw is undersized.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Growth Factor Complex 200 GFC 200 Recalled by EonNutra, LLC Due to Eon...
The Issue: Eon Nutra, LLC is recalling certain SOTO Supplements GFC 200 because the...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Coca-Cola Recalled by Coca-Cola Company (The) Due to Complaints received of...
The Issue: Complaints received of off taste/odor.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: The Lumenis VersaCut Tissue Morcellator Product Usage: is intended for...
The Issue: Lumenis Ltd is recalling certain models of VersaCut Morcellator devices to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Diagnostic Hybrids Recalled by Diagnostic Hybrids Inc Due to RhMK product...
The Issue: RhMK product fungal contamination.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Rugby NATURAL IRON SUPPLEMENT Ferrous Sulfate Recalled by Advance...
The Issue: Labeling; Label Mixup; bottles of Ferrous Sulfate actually contains...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.