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. 2,832 recalls have been distributed to Florida in the last 12 months.
Showing 16081–16100 of 55,837 recalls
Recalled Item: TRUMATCH CT PIN GUIDE KIT L- TruMatch Patient Specific Instruments Recalled...
The Issue: Software: A coding error associated with the Fast3D Segmentation software....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Marketside Chocolate Candy Cookie Cake Recalled by Jimmy's Cookies, LLC Due...
The Issue: Undeclared allergen - Peanuts.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Bivona Aire-Cuf Endotracheal Tube Recalled by Smiths Medical ASD Inc. Due to...
The Issue: Inadequate pouch seal leading to a compromised sterile barrier on products...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bivona Uncuffed Wire Endotracheal Tubes Recalled by Smiths Medical ASD Inc....
The Issue: Inadequate pouch seal leading to a compromised sterile barrier on products...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Access hsTnI High Sensitivity Troponin I Recalled by Beckman Coulter Inc....
The Issue: Through customer feedback, testing a sample with cardiac troponin I...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ad-Tech Lightweight TECH ATTACH Cable - Product Usage: Designed for Recalled...
The Issue: Incorrect version of labels were used.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ad-Tech Lightweight CABRIO Cable - Product Usage: Designed for the Recalled...
The Issue: Incorrect version of labels were used.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ad-Tech TECH ATTACH Cable- Product Usage: Designed for the purpose Recalled...
The Issue: Incorrect version of labels were used.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Micafungin for Injection Recalled by XELLIA PHARMACEUTICALS USA, LLC Due to...
The Issue: Labeling; Incorrect or Missing Package Insert: The package insert provided...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Micafungin for Injection Recalled by XELLIA PHARMACEUTICALS USA, LLC Due to...
The Issue: Labeling; Incorrect or Missing Package Insert: The package insert provided...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Fermentation Derived Pepsin Product packaging: 5 individual LDPE bags with...
The Issue: Undeclared egg allergen
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Zoll Recalled by ZOLL Circulation, Inc. Due to Labeling update concerning...
The Issue: Labeling update concerning potential leaks from the catheter or the start-up...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ion Flexison Biopsy Needle Recalled by Intuitive Surgical, Inc. Due to...
The Issue: Potential for the sheath tip on the biopsy needle to separate from the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ZOLL Recalled by ZOLL Circulation, Inc. Due to Labeling update concerning...
The Issue: Labeling update concerning potential leaks from the catheter or the start-up...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ZOLL Recalled by ZOLL Circulation, Inc. Due to Labeling update concerning...
The Issue: Labeling update concerning potential leaks from the catheter or the start-up...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zoll Recalled by ZOLL Circulation, Inc. Due to Labeling update concerning...
The Issue: Labeling update concerning potential leaks from the catheter or the start-up...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zoll Recalled by ZOLL Circulation, Inc. Due to Labeling update concerning...
The Issue: Labeling update concerning potential leaks from the catheter or the start-up...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TECNIS Eyhance IOLs are permanent intraocular implants intended for...
The Issue: Nonconforming product was distributed in error. Product was nonconforming...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zoll (SL-2593CO) Recalled by ZOLL Circulation, Inc. Due to Labeling update...
The Issue: Labeling update concerning potential leaks from the catheter or the start-up...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ZOLL Recalled by ZOLL Circulation, Inc. Due to Labeling update concerning...
The Issue: Labeling update concerning potential leaks from the catheter or the start-up...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.