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. 2,096 recalls have been distributed to Florida in the last 12 months.
Showing 7961–7980 of 30,686 recalls
Recalled Item: Amplatz extra Stiff Wire Guide Recalled by Cook Incorporated Due to Cook...
The Issue: Cook Medical identified that devices from the affected device lots may have...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ConvaTec Esteem+ Durahesive Plus Recalled by ConvaTec, Inc Due to impaired...
The Issue: impaired functionality of the release liner
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Roadrunner PC Wire Guide (The Firm LT) Recalled by Cook Incorporated Due to...
The Issue: Cook Medical identified that devices from the affected device lots may have...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bentson Plus Wire Guide (Extra Body/20cm Distal Flexibility with Softened...
The Issue: Cook Medical identified that devices from the affected device lots may have...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Newton Wire Guide (LT Taper/10cm Distal Flexibility) Recalled by Cook...
The Issue: Cook Medical identified that devices from the affected device lots may have...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ConvaTec Esteem+ Durahesive Plus Recalled by ConvaTec, Inc Due to impaired...
The Issue: impaired functionality of the release liner
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ConvaTec Active Life Recalled by ConvaTec, Inc Due to impaired functionality...
The Issue: impaired functionality of the release liner
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Olympus POWERSEAL 5MM Recalled by Olympus Corporation of the Americas Due to...
The Issue: An out of specification component preventing the blue retention ring from...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EMPOWER 3D Knee Tibial Insert Recalled by Encore Medical, LP Due to Hip...
The Issue: Hip liner implant boxes may contain knee inserts and knee insert boxes may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Olympus POWERSEAL 5MM Recalled by Olympus Corporation of the Americas Due to...
The Issue: An out of specification component preventing the blue retention ring from...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DeRoyal Sterile Custom Kits containing ICU Medical MicroClave Clear...
The Issue: Procedure packs contained a recalled product.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Humidifier bottle and syringe filter kit (6 count of each) Recalled by...
The Issue: There is a potential breach to the sterile barrier containing the Humidifier...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Olympus POWERSEAL 5MM Recalled by Olympus Corporation of the Americas Due to...
The Issue: An out of specification component preventing the blue retention ring from...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Humidifier bottle and syringe filter kit (6 count of each) Recalled by...
The Issue: There is a potential breach to the sterile barrier containing the Humidifier...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EMPOWR Acetabular System Recalled by Encore Medical, LP Due to Hip liner...
The Issue: Hip liner implant boxes may contain knee inserts and knee insert boxes may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sedecal Soltus Battery Mobile X-Ray System 450 Battery Recalled by SEDECAL...
The Issue: Due to un-commanded movement of mobile x-ray unit.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GXL acetabular liners Recalled by Exactech, Inc. Due to Specific GXL...
The Issue: Specific GXL acetabular polyethylene liners, packaged in non-conforming...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GXL acetabular liners Recalled by Exactech, Inc. Due to Specific GXL...
The Issue: Specific GXL acetabular polyethylene liners, packaged in non-conforming...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GXL acetabular liners Recalled by Exactech, Inc. Due to Specific GXL...
The Issue: Specific GXL acetabular polyethylene liners, packaged in non-conforming...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GXL acetabular liners Recalled by Exactech, Inc. Due to Specific GXL...
The Issue: Specific GXL acetabular polyethylene liners, packaged in non-conforming...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.