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. 2,723 recalls have been distributed to Florida in the last 12 months.
Showing 24301–24320 of 30,686 recalls
Recalled Item: ANSPACH - Fluted Acorn Recalled by The Anspach Effort, Inc. Due to G1...
The Issue: G1 Dissection Tools are not compatible with all attachments listed on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ANSPACH - 4MM Diamond Ball Recalled by The Anspach Effort, Inc. Due to G1...
The Issue: G1 Dissection Tools are not compatible with all attachments listed on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ANSPACH - Fluted Drum Recalled by The Anspach Effort, Inc. Due to G1...
The Issue: G1 Dissection Tools are not compatible with all attachments listed on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ANSPACH - 5MM Diamond Ball Recalled by The Anspach Effort, Inc. Due to G1...
The Issue: G1 Dissection Tools are not compatible with all attachments listed on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ANSPACH - Fluted Barrel Recalled by The Anspach Effort, Inc. Due to G1...
The Issue: G1 Dissection Tools are not compatible with all attachments listed on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ANSPACH - 8MM x 12.5MM Fluted Barrel Recalled by The Anspach Effort, Inc....
The Issue: G1 Dissection Tools are not compatible with all attachments listed on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EPIQ 7 Ultrasound System with Pediatric Cardiology option Recalled by...
The Issue: When Epiq 7 Ultrasound System, WITH the Pediatric Cardiology option, is set...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EPIQ 5 Ultrasound System with Pediatric Cardiology option Recalled by...
The Issue: When Epiq 5 Ultrasound System, WITH the Pediatric Cardiology option, is set...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic SynchroMed II Implantable Infusion Pumps Recalled by Medtronic...
The Issue: Medtronic is conducting a recall of a specific subset of Model 8637-20 and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 4.0mm Variable Angle Recalled by Alphatec Spine, Inc. Due to Mislabeling
The Issue: During a field audit it was discovered by an employee that a 16mm Trestle...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BARD MAX-CORE Disposable Core Biopsy Instrument Gauge x Length 18g Recalled...
The Issue: The firm is recalling Bard MAX-CORE Disposable Core Biopsy Instrument due to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Genesis Malleable Penile Prosthesis Recalled by Coloplast Manufacturing US,...
The Issue: Several lots of the 9.5 mm Genesis Malleable Penile Prosthesis were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TFN-ADVANCED Proximal Femoral Nailing System (TFNA) Recalled by Synthes,...
The Issue: TFNA nails from certain lots were assembled with a locking mechanism too...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Spinal Elements 5.5 x 45MM Mercury lordosed rod. A component Recalled by...
The Issue: Some rods may not meet the appropriate traceability requirements including...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Primus (THE BTE WS30) Recalled by BTE Technologies, Inc. Due to On the...
The Issue: On the Primus that includes the optional Chop / Lift Bar, there is a remote...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ABACUS SE (Single-Workstation Edition) and ABACUS ME (Multi-Workstation...
The Issue: Baxter Corporation is conducting a field action for the ABACUS SE and ME...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fortex" Pedicle Screw System Continuous Radius Rod 5.5 - 50mm Recalled by X...
The Issue: The Continuous Radius Rod should measure 50mm in length but actually...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HSG Trays/HS 5F Catheter Combo Recalled by Catheter Research, Inc Due to...
The Issue: HSG Trays and Catheters were mislabeled. Trays with the flexible HS catheter...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS 4600 Chemistry System Recalled by Ortho-Clinical Diagnostics Due to...
The Issue: Software anomaly allows testing of multiple assays using a single urine...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS 5 Recalled by Ortho-Clinical Diagnostics Due to Software anomaly...
The Issue: Software anomaly regarding urine samples that require acidified...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.