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. 1,830 recalls have been distributed to Florida in the last 12 months.
Showing 41441–41460 of 55,837 recalls
Recalled Item: Volcano s5/s5i/CORE Intravascular Ultrasound Systems software versions 3.3...
The Issue: A software issue was discovered where an inaccurate FFR/iFR value could be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Volcano s5/s5i/CORE Intravascular Ultrasound Systems software versions 3.3...
The Issue: A software issue was discovered where an inaccurate FFR/iFR value could be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Abutment Retrieval Instrument Zirconia CC RP/WP Recalled by Nobel Biocare...
The Issue: One dimension of the affected instrument is incorrect. Therefore this...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Volcano s5/s5i/CORE Intravascular Ultrasound Systems software versions 3.3...
The Issue: A software issue was discovered where an inaccurate FFR/iFR value could be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fabius MRI Anesthesia Machine Recalled by Draeger Medical, Inc. Due to the...
The Issue: the Fabius MRI or parts of the system were attracted by the magnetic field...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Volcano s5/s5i/CORE Intravascular Ultrasound Systems with software versions...
The Issue: A software issue was discovered where an inaccurate FFR/iFR value could be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Milex Vaginal-Hymenal Silicone Dilators Set of 4 P/N MX20 Product Recalled...
The Issue: Incorrect expiration date on outer carton kit label
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sour Caramel Apple Chewing Recalled by Project 7 Due to Undeclared Milk
The Issue: Project 7 is recalling all lots of Sour Caramel Apple Chewing Gum because...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Acadia Natural Spring Water Recalled by Niagara Bottling, LLC Due to...
The Issue: Source Spring Water was analyzed and found positive for E. coli and total...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Disulfiram tablets Recalled by Qualitest Pharmaceuticals Due to Failed...
The Issue: Failed Dissolution Specifications: During routine stability testing at the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Sysco International Whole Segments Mandarin Oranges In Light Syrup Net...
The Issue: Product tested positive for Carbendazim.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Mission -Breath Alcohol Detector -15 tests - 0.08% BAC - Recalled by Acon...
The Issue: Acon Laboratories, Inc. is recalling Mission Breath Alcohol Detector due to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Invivo Expression MRI Patient Monitoring System. Recalled by Philips...
The Issue: The device's labeling inaccurately indicates Endotracheal as a body...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arthroscopic Energy 50¿ Probe with Suction Recalled by ConMed Corporation...
The Issue: Probe programming error. The incorrect program can generate more heat at the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: INSTRUMENT ARM DRAPE Recalled by Intuitive Surgical, Inc. Due to Field...
The Issue: Field Safety Notification to advise of an issue that may occur involving the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SYMMETRY SURGICAL DISPOSABLE TOWEL CLAMP Recalled by Symmetry Surgical, Inc....
The Issue: Lack of sterility assurance.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OPD-Scan III Power/Corneal Analyzer Opthalmic Software versions 1.00.08...
The Issue: Software bug was found where there was no difference in Total and Corneal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Block Versions Used by Dental Offices often to as Recalled by 3M Company -...
The Issue: 3M is initiating a Field Correction to remove the crown indication from all...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Slipped Capital Femoral Epiphysis (SCFE) Drivers of the Free-Gliding SCFE...
The Issue: SCFE Drivers of the Free-Gliding SCFE Screw System are recalled because the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mermaid Medical M-Biopsy Coaxial Introducer Needle Recalled by Mermaid...
The Issue: Mermaid Medical A/S is recalling some of their M-Biopsy Coaxial Introducer...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.