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. 2,939 recalls have been distributed to Florida in the last 12 months.
Showing 2241–2260 of 30,686 recalls
Recalled Item: Access 2 Immunoassay Analyzer Recalled by Beckman Coulter, Inc. Due to...
The Issue: Beckman Coulter identified that an issue for Access 2 Sample Motors (B48016)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Aortic Root Cannula: 1. DLP Aortic Root Cannula A. CANNULA Recalled by...
The Issue: Unexpected loose material in the male luer used in the aortic root cannula...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Rotarex Atherectomy System and Instructions for Use Recalled by Bard...
The Issue: Atherectomy Catheter eIFU updated to clarify and emphasize procedural steps...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Baxter Sigma Spectrum Infusion System (V6 Platform) Recalled by Baxter...
The Issue: There is the potential for missing motor mounting screws, which may have...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Baxter Spectrum IQ Infusion System with Dose IQ Safety Software Recalled by...
The Issue: There is the potential for missing motor mounting screws, which may have...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IntelePACS (Image Fusion Module) - InteleViewer Recalled by INTELERAD...
The Issue: A software application that receives digital images and data from various...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IsoLoc Short Profile Prostate Immobilization Treatment Balloon Device Kit...
The Issue: Product is mislabeled with the incorrect fill volume.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HemosIL LMW Heparin Controls Recalled by Instrumentation Laboratory Due to...
The Issue: Multiple complaints indicating lower than expected quality control (QC)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CardioMEMS Heart Failure (HF) System that consist of: -CardioMEMS Hospital...
The Issue: Due to issues associated with data migration of patient information and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: TBS Osteo Product Name: TBS iNsight Model/Catalog Number:...
The Issue: Potential variability in calculations from fast array scans compared to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Access Erythropoietin (EPO) Recalled by Beckman Coulter, Inc. Due to...
The Issue: Affected lot (439363) exhibited a negative dose drop of -22% with native...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Numerous models of nonsterile hemostatic forceps: (1) Recalled by Aesculap...
The Issue: The forceps have been used in ways not covered by the design resulting in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Numerous models of nonsterile hemostatic forceps: (1) Recalled by Aesculap...
The Issue: The forceps have been used in ways not covered by the design resulting in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Numerous models of nonsterile hemostatic forceps: (1) Recalled by Aesculap...
The Issue: The forceps have been used in ways not covered by the design resulting in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Numerous models of nonsterile hemostatic forceps: (1) Recalled by Aesculap...
The Issue: The forceps have been used in ways not covered by the design resulting in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Numerous models of nonsterile hemostatic forceps: (1) Recalled by Aesculap...
The Issue: The forceps have been used in ways not covered by the design resulting in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MiniMed insulin pump Recalled by Medtronic MiniMed, Inc. Due to All...
The Issue: All Medtronic MiniMed pumps (Paradigm series, Minimed 530G, 6XX series, and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SIGNA MR355 Recalled by GE Healthcare (China) Co., Ltd. Due to For certain...
The Issue: For certain MR systems, a scan can be resumed following a Power Monitor trip...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MiniMed insulin pump Recalled by Medtronic MiniMed, Inc. Due to All...
The Issue: All Medtronic MiniMed pumps (Paradigm series, Minimed 530G, 6XX series, and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MiniMed insulin pump Recalled by Medtronic MiniMed, Inc. Due to All...
The Issue: All Medtronic MiniMed pumps (Paradigm series, Minimed 530G, 6XX series, and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.