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. 2,815 recalls have been distributed to Florida in the last 12 months.
Showing 17181–17200 of 30,686 recalls
Recalled Item: Unify Assura Recalled by St Jude Medical Inc. Due to The firm is releasing...
The Issue: The firm is releasing new firmware for high voltage implantable cardiac...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Quadra Assura Recalled by St Jude Medical Inc. Due to The firm is releasing...
The Issue: The firm is releasing new firmware for high voltage implantable cardiac...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AMENDIA Omega Lumbar Interbody Fusion Device Recalled by Spinal Elements Due...
The Issue: Omega LIF interbody implants labeled as having 11 degrees of lordosis was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ATTUNE Revision CRS Femoral RT SZ 5 Cemented Recalled by DePuy Orthopaedics,...
The Issue: There may be burrs on the extraction hole threads.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BARD PERIPHERAL VASCULAR SEEKER(R) Crossing Support Catheter Recalled by...
The Issue: Device is at risk of having detectable levels of bacterial endotoxin present...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BARD PERIPHERAL VASCULAR SEEKER(R) Crossing Support Catheter Recalled by...
The Issue: Device is at risk of having detectable levels of bacterial endotoxin present...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ATTUNE Revision CRS Femoral LT SZ 5 Cemented Recalled by DePuy Orthopaedics,...
The Issue: There may be burrs on the extraction hole threads.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Advance¿ 35LP Low-Profile PTA Balloon Dilatation Catheter Recalled by Cook...
The Issue: Incorrect product labeling. Product labeled as 6mm x 2cm balloon are...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Merlin PCS Programmer software model 3330 Recalled by St Jude Medical,...
The Issue: Devices inappropriately displayed a low battery indicator determined to be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alaris Pump Recalled by CareFusion 303, Inc. Due to The bezel manufacturing...
The Issue: The bezel manufacturing process for the FR-110 plastic may have resulted in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CSI Recalled by Cardiovascular Systems Inc Due to The pumps may switch to...
The Issue: The pumps may switch to stand-by during use requiring the pump to be reset...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medfusion Syringe Infusion Pump Recalled by Smiths Medical ASD Inc. Due to...
The Issue: Certain Barrel Clamp Guides may contain a ridge that could potentially lead...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Nitinol Staple Recalled by TriMed Inc. Due to During a retrospective review...
The Issue: During a retrospective review of sterilization records, TriMed has...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Nitinol Staple Recalled by TriMed Inc. Due to During a retrospective review...
The Issue: During a retrospective review of sterilization records, TriMed has...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Nitinol Staple Recalled by TriMed Inc. Due to During a retrospective review...
The Issue: During a retrospective review of sterilization records, TriMed has...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Nitinol Staple Recalled by TriMed Inc. Due to During a retrospective review...
The Issue: During a retrospective review of sterilization records, TriMed has...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FlowGate2 Balloon Guide Catheter Recalled by Stryker Neurovascular Due to...
The Issue: There may be product manufactured with the outer diameter of the balloon...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 4Fr. Catheter Clamp with Fastener Recalled by Arrow International Inc Due to...
The Issue: Product sterility may be compromised due to unsealed packaging.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 8Fr. Catheter Clamp with Fastener Recalled by Arrow International Inc Due to...
The Issue: Product sterility may be compromised due to unsealed packaging.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Maximal Barrier Drape Recalled by Arrow International Inc Due to Product...
The Issue: Product sterility may be compromised due to unsealed packaging.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.