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. 2,801 recalls have been distributed to Florida in the last 12 months.
Showing 17461–17480 of 30,686 recalls
Recalled Item: Medtronic Prestige LP(TM) Cervical Disc System with Streamlined Instruments...
The Issue: The firm received complaints of drill bits breaking during use with the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Genesis Surgical Cassette Tapered Implants are intended for placement...
The Issue: The surgical cassette contained extra-large white grommets making the 3.8 mm...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 5 mm Apple-Hunt Secondary Cannula/Pyramidal Tip Trocar - extended length...
The Issue: Products have been packaged with the wrong Trocar length type.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hamilton-C3 Ventilator Unit Intended to provide ventilator support to adults...
The Issue: After two and a half years, the battery fuel gauge may indicate a higher...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Power-LOAD Cot Fastening System Recalled by Stryker Medical Division of...
The Issue: The power load floor plates which hold the ambulance cot anchors in place...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Phoenix Nail System Recalled by Zimmer Biomet, Inc. Due to Certain lots of...
The Issue: Certain lots of the Phoenix Tibia Nail 3.5mm Inserter instruments are being...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hinge Coupling Hoffmann LRF Catalog # 4933-0-800 Intended for fixation...
The Issue: The wrong parts were picked for packaging. The connecting Nuts were packed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hamilton-C2 Ventilator Unit Intended to provide ventilator support to adults...
The Issue: After two and a half years, the battery fuel gauge may indicate a higher...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Syva¿ EMIT¿ II Plus 6-Acetylmorphine Catalog # for 1000 mL: Recalled by...
The Issue: Incorrect calibrator level listed in qualitative calibration steps
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: McKesson Cardiology Hemo Recalled by McKesson Israel Ltd. Due to Change...
The Issue: Change Healthcare has identified an issue where, under certain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vacuum Regulator Recalled by Ohio Medical Corporation Due to Final quality...
The Issue: Final quality control testing was not completed before the devices were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Syva¿ EMIT¿ II Plus 6-Acetyl morphine Catalog # for 28 Recalled by Siemens...
The Issue: Incorrect calibrator level listed in qualitative calibration steps
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Edwards Lifesciences Avid Dual Stage Venous Drainage Cannula Recalled by SPS...
The Issue: The expiration date on the device labeling exceeds its actual validated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Edwards Lifesciences Optisite Arterial Perfusion Cannula Recalled by SPS...
The Issue: The expiration date on the device labeling exceeds its actual validated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Boston Scientific Wallstent Endoprosthesis Tracheobronchial Self-Expanding...
The Issue: The expiration date on the device labeling exceeds its actual validated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Boston Scientific Wallstent RP Endoprosthesis Tracheobronchial Transhepatic...
The Issue: The expiration date on the device labeling exceeds its actual validated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Edwards Lifesciences Femoral Venous Cannula Recalled by SPS Sterilization,...
The Issue: The expiration date on the device labeling exceeds its actual validated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Boston Scientific Wallstent Endoprosthesis Tracheobronchial Transhepatic...
The Issue: The expiration date on the device labeling exceeds its actual validated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: da Vinci X Surgical System Recalled by Intuitive Surgical, Inc. Due to...
The Issue: Specific da Vinci X Surgical Systems (IS4200) were shipped with defective...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Boston Scientific Wallstent Endoprosthesis Tracheobronchial Self-Expanding...
The Issue: The expiration date on the device labeling exceeds its actual validated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.