Product Recalls in Georgia
Product recalls affecting Georgia — including food, drugs, consumer products, medical devices, and vehicles distributed to Georgia. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,842 recalls have been distributed to Georgia in the last 12 months.
Showing 3961–3980 of 29,505 recalls
Recalled Item: Philips Tempus LS-Manual Defibrillator Recalled by Remote Diagnostic...
The Issue: Simultaneous ECG measurements with multiple devices, including a manual...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Multitest 6-Color TBNK CE-IVD Recalled by Becton, Dickinson and Company,...
The Issue: Multitest with compromised raw material used to assess immune system status...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Centrella Max - The Centrella Smart+ Bed is intended for Recalled by Baxter...
The Issue: There is a potential for the top cover of the hospital bed mattress to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Thoratec HeartMate System Monitor Recalled by Thoratec Corp. Due to System...
The Issue: System monitor screen may display atypical behavior: Overlapping...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
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.