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. 2,710 recalls have been distributed to Florida in the last 12 months.
Showing 26601–26620 of 55,837 recalls
Recalled Item: Bupropion Hydrochloride ER Tablets Recalled by InvaGen Pharmaceuticals, Inc....
The Issue: Failed impurities/ degradation specifications: Out-of-specification results...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Pramipexole dihydrochloride extended release tablets Recalled by Par...
The Issue: Failed impurities/degradation specifications: Finished product contain a...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: 0.9% Sodium Chloride Injection USP 50 mL Viaflex container Baxter Recalled...
The Issue: cGMP Deviation
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Heating Profile PRISMAFLO II blood return warmer for Prismaflex Product...
The Issue: PRISMAFLO II and PRISMAFLO II S Heating Profile only and not the Control...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CryoPatch SG Pulmonary Hemi-Artery Recalled by CryoLife, Inc. Due to The...
The Issue: The conduit length and branch length of a SG Pulmonary Hemi-Artery were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Implant Direct Scan Adapter Assembly Replant platform for the following...
The Issue: The action is being initiated due to incorrect assembly of the scan adapter...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Altrix¿ Precision Temperature Management System Model: 8001Product Usage:...
The Issue: Users may experience alarm fatigue due to frequent alarming relating to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Heating Profile PRISMAFLO II S blood return warmer for Prismaflex Recalled...
The Issue: PRISMAFLO II and PRISMAFLO II S Heating Profile only and not the Control...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Heating Profile PRISMAFLO II S blood return warmer for Prismaflex Recalled...
The Issue: PRISMAFLO II and PRISMAFLO II S Heating Profile only and not the Control...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cordis POWERFLEX PRO PTA Dilatation Catheter - Product Usage: Is Recalled by...
The Issue: Product may not meet the internal manufacturing shaft subassembly burst...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FilmArray Blood Culture Identification (BCID) Recalled by BioFire...
The Issue: Increased risk of false positive results for Proteus when the product is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Thoratec CentriMag Motor Recalled by Thoratec Switzerland GMBH Due to...
The Issue: Reports of circulatory support system motor stopping. Motor stop can be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Colpo-Pneumo Occluder Recalled by CooperSurgical, Inc. Due to The seal of...
The Issue: The seal of the sterile pouch may be compromised, thereby increasing the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Neuro Omega System Recalled by Alpha Omega Engineering Due to If cables are...
The Issue: If cables are improperly connected, current may reach high charge density,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Retractor System Elastic Stays (Part 3314-lG Recalled by CooperSurgical,...
The Issue: There is a possibility that the seal of the sterile pouch may be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare CARESCAPE Monitor B850 Product Usage: Intended uses of...
The Issue: When multiple CARESCAPEMonitor B450 or B850 units are connected to the same...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vereos PET/CT Recalled by Philips Medical Systems (Cleveland) Inc Due to...
The Issue: Software Correction: Software errors that may result in incorrect 4D CT...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare CARESCAPE Monitor B450 Product Usage: Intended uses of...
The Issue: When multiple CARESCAPEMonitor B450 or B850 units are connected to the same...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hemotherm 400CE Recalled by Cincinnati Sub-Zero Products LLC, a Gentherm...
The Issue: Potential for membrane (control panel) switch errors leading to an inability...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: McKesson Insulin Syringe 0.3mL 31GX5/16 Item Numbers: 102-SN310C31516P...
The Issue: Small hole at the end of the syringe is impeding suction of liquid.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.