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. 2,768 recalls have been distributed to Florida in the last 12 months.
Showing 18321–18340 of 30,686 recalls
Recalled Item: Monarch Airway Clearance System Recalled by HILL-ROM MANUFACTURING, INC. Due...
The Issue: Monarch Electromagnetic Interference (EMI) may disrupt the operation of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Personal Intermittent Catheters- 16" and 10" lengths - 30 catheters per box...
The Issue: Several instances of a catheter caught in the sterile barrier seal and in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Magic 3 Intermittent Catheters- 12 Male - 30 catheters per box Recalled by...
The Issue: Several instances of a catheter caught in the sterile barrier seal and in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Peripheral Diamondback 1.50 Solid OAD Recalled by Cardiovascular Systems Inc...
The Issue: Cardiovascular Systems, Inc. (CSI) is removing the products because it was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Peripheral Diamondback 1.25 Solid OAD Recalled by Cardiovascular Systems Inc...
The Issue: Cardiovascular Systems, Inc. (CSI) is removing the products because it was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HydroSil Gripper Intermittent Catheters- 10" lengths - 30 catheters per box...
The Issue: Several instances of a catheter caught in the sterile barrier seal and in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 14-442000S Antegrade Femoral Nail Instrument Kit Recalled by Zimmer Biomet,...
The Issue: Fracture of the bolt connecting the insertion guide to the intramedullary...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Aptus Heli-FX Thoracic EndoAnchor System Heli-FX Guide 42 mm...
The Issue: It was determined that the deflection length indicated on the Guide catheter...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SECURE(R) 100mL EMPTY VINYL CONTAINER With 2 Ports - (5 Boxes of 40)...
The Issue: The hot stamp label on the bag incorrectly states the material of the vinyl...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 979195 Loaner Kit for femoral intramedullary nail. Orthopedic instrument....
The Issue: Fracture of the bolt connecting the insertion guide to the intramedullary...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Phoenix Antegrade Femoral Nail Trochanteric and Piriformis fossa Recalled by...
The Issue: Fracture of the bolt connecting the insertion guide to the intramedullary...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Infinity 5 Implantable Pulse Generator and Infinity 7 Implantable Pulse...
The Issue: Analysis of the difference between the actual device longevity and the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Proclaim 5 Elite Implantable Pulse Generator and Proclaim 7 Elite Recalled...
The Issue: Analysis of the difference between the actual device longevity and the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: i-STAT DE handheld data processing module for clinical use Recalled by...
The Issue: Issues resulting from upgrade to software version 2.8: (1) Location,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Toshiba Medical Kalare Fluoroscopic X-Ray System (DREX-KL80) Kalare is...
The Issue: During an examination images were displayed on the live monitor,but the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LifeVest Wearable Defibrillator Model 4000 Recalled by Zoll Manufacturing...
The Issue: Incorrect service code for properly catching critical defects during...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Proclaim DRG Implantable Pulse Generator Model 3664 Recalled by St. Jude...
The Issue: Analysis of the difference between the actual device longevity and the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BlockAid Cut Resistant Surgical Glove Liners Recalled by Zimmer Biomet, Inc....
The Issue: Cut resistant surgical glove liners lack sterility assurance.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sysmex Fluorocell(R) PLT Fluorocell PLT is used to stain platelets Recalled...
The Issue: There is potential that fluorescent platelet (PLT-F) and immature platelet...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AutoCheck5+ Recalled by Radiometer America Inc Due to Radiometer has...
The Issue: Radiometer has recently become aware that a few of the AUTOCHECK 5+ level 2...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.