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. 2,923 recalls have been distributed to Florida in the last 12 months.
Showing 4021–4040 of 30,686 recalls
Recalled Item: MEGADYNE MEGA SOFT Pediatric Patient Return Electrode. Reusable Patient...
The Issue: Reports of patient burns.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS Immunodiagnostic Products Vitamin B12 Range Verifier - In vitro...
The Issue: The results generated by the VITROS Immunodiagnostic Products Vitamin B12...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline ReNewal Reprocessed Covidien LigaSure Maryland Jaw Sealer/Divider...
The Issue: Potential for an incomplete seal on the packaging tray.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline ReNewal Reprocessed Covidien LigaSure Blunt Tip Recalled by MEDLINE...
The Issue: Potential for an incomplete seal on the packaging tray.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline ReNewal Reprocessed Covidien LigaSure Impact Recalled by MEDLINE...
The Issue: Potential for an incomplete seal on the packaging tray.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline ReNewal Reprocessed Ethicon Harmonic ACE+7 Shears w/ Adv. Hemostasis...
The Issue: Potential for an incomplete seal on the packaging tray.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Replacement Battery List Number SUB0000594 and SUB0000864 found in Plum...
The Issue: Due to a manufacturing defect from the battery supplier, affected batteries...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Plum 360/A+ spare batteries. Item Number: SUB0000864. Recalled by ICU...
The Issue: Due to a manufacturing defect from the battery supplier, affected batteries...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Replacement Battery List Number SUB0000864 Recalled by ICU Medical Inc Due...
The Issue: Due to a manufacturing defect from the battery supplier, affected batteries...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CORI Starter Kit Recalled by Blue Belt Technologies, Inc Due to CORI...
The Issue: CORI Surgical System with Real Intelligence Software exhibits an increased...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CODMAN BACTISEAL EVD Catheter Set - Indicated for gaining access Recalled by...
The Issue: Defect in the external sterile packaging (pouch) leading to a gap or/and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CODMAN BACTISEAL Clear EVD Catheter 1.9mm I.D. Catheter Set- indicated...
The Issue: Defect in the external sterile packaging (pouch) leading to a gap or/and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CODMAN EVD BACTISEAL 1.9mm I.D. Catheter Set- indicated for gaining Recalled...
The Issue: Defect in the external sterile packaging (pouch) leading to a gap or/and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD SARS-CoV-2 Reagents for BD MAX" Systems. RT-PCR test to Recalled by...
The Issue: Assays may produce false negative results due to decreased activity of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: American Contract Systems Spine Pack convenience kit Recalled by American...
The Issue: Product released with insufficient aeration time impacting the kits...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: American Contract Systems Hand Pack convenience kit Recalled by American...
The Issue: Product released with insufficient aeration time impacting the kits...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: American Contract Systems Biopsy Drape Pack convenience kit Recalled by...
The Issue: Product released with insufficient aeration time impacting the kits...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: American Contract Systems Laparoscopy Litho Std Pack convenience kit and...
The Issue: Product released with insufficient aeration time impacting the kits...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: American Contract Systems Special Procedure Pack convenience kit Recalled by...
The Issue: Product released with insufficient aeration time impacting the kits...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: American Contract Systems Cataract Pack convenience kit Recalled by American...
The Issue: Product released with insufficient aeration time impacting the kits...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.