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. 2,858 recalls have been distributed to Georgia in the last 12 months.
Showing 3261–3280 of 53,623 recalls
Recalled Item: Nelarabine Injection Recalled by Zydus Pharmaceuticals (USA) Inc Due to...
The Issue: Failed Impurities/Degradation Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Nelarabine Injection Recalled by Zydus Pharmaceuticals (USA) Inc Due to...
The Issue: Failed Impurities/Degradation Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Proxima Drape labeled as PACK Recalled by MEDLINE INDUSTRIES, LP -...
The Issue: Potential breach in pouch packaging which could lead to loss of sterility.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Proxima Drape labeled as ORTHO TRAUMA CDS Recalled by MEDLINE INDUSTRIES, LP...
The Issue: Potential breach in pouch packaging which could lead to loss of sterility.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Proxima Drape labeled as UNIVERSAL DAVINCI ROBOTIC P. Sterile surgical...
The Issue: Potential breach in pouch packaging which could lead to loss of sterility.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Proxima Drape labeled as HEAD AND NECK OSIS Recalled by MEDLINE INDUSTRIES,...
The Issue: Potential breach in pouch packaging which could lead to loss of sterility.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Proxima Drape labeled as MINOR PACK and LAPAROSCOPY. Sterile surgical drape....
The Issue: Potential breach in pouch packaging which could lead to loss of sterility.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Proxima Drape labeled as ENT-PLASTICS PACK. Sterile surgical drape. Recalled...
The Issue: Potential breach in pouch packaging which could lead to loss of sterility.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Proxima Drape labeled as DRAPE C-SECTION W/ WINDOW Recalled by MEDLINE...
The Issue: Potential breach in pouch packaging which could lead to loss of sterility.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Proxima Drape labeled as FACE LIFT. Sterile surgical drape. Recalled by...
The Issue: Potential breach in pouch packaging which could lead to loss of sterility.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: ZOLL Product Name: Powerheart G5 AED Model/Catalog Number:...
The Issue: The potential for devices to fail their self-test as a result of prolonged...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: ZOLL Product Name: Powerheart G5 AED Model/Catalog Number:...
The Issue: The potential for devices to fail their self-test as a result of prolonged...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: ZOLL Product Name: Powerheart G5 AED Model/Catalog Number:...
The Issue: The potential for devices to fail their self-test as a result of prolonged...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: ZOLL Product Name: Powerheart G5 AED Model/Catalog Number:...
The Issue: The potential for devices to fail their self-test as a result of prolonged...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: ZOLL Product Name: Powerheart G5 AED Model/Catalog Number:...
The Issue: The potential for devices to fail their self-test as a result of prolonged...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: ZOLL Product Name: Powerheart G5 AED Model/Catalog Number:...
The Issue: The potential for devices to fail their self-test as a result of prolonged...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Portex Endotracheal Tube Recalled by Smiths Medical ASD, Inc. Due to...
The Issue: Affected devices have a smaller diameter than expected and may potentially...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: ZOLL Product Name: Powerheart G5 AED Model/Catalog Number:...
The Issue: The potential for devices to fail their self-test as a result of prolonged...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: ZOLL Product Name: Powerheart G5 AED Model/Catalog Number:...
The Issue: The potential for devices to fail their self-test as a result of prolonged...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: remel BLOOD AGAR EMB AGAR BIPLATE Recalled by Remel, Inc Due to Potential...
The Issue: Product may contain surface and subsurface contamination of Listeria...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.