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 23661–23680 of 30,686 recalls
Recalled Item: 30inch Dual Port/Single Bladder Disposable Tourniquet Cuff with PLC Recalled...
The Issue: The inside of the folded Instructions For Use (IFU) pamphlet was missing the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synthes TI Matrix Pre-Bent Maxillary Plate / 2mm ADVMNT/0.8mm THK/L Recalled...
The Issue: The affected part and lot numbers of the TI Matrix Pre-Bent Maxillary Plates...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 16mm Chisel Blade Recalled by Synthes (USA) Products LLC Due to It was...
The Issue: It was discovered that a 10mm Chisel Blade was etched as a 16mm Chisel Blade.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The EKOS EkoSonic Control Unit is intended exclusively for use Recalled by...
The Issue: The Connector Interface Cable (CIC) was not recognized by the EkoSonic PT-3B...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Vacutainer SST Plus Blood Collection Tubes Recalled by Becton Dickinson &...
The Issue: Some of the tubes were manufactured with stoppers that did not meet current...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: O-Two Adult Ventilation Timer Recalled by O-Two Medical Technologies, Inc....
The Issue: Malfunction of an O-Two Adult Ventilation Timer, where the flash rate of the...
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: 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: 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: 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: 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: 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: 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: 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: 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: 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.