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. 2,661 recalls have been distributed to Georgia in the last 12 months.
Showing 23781–23800 of 53,623 recalls
Recalled Item: Monoject Blunt Cannula Recalled by Cardinal Health 200, LLC Due to...
The Issue: Manufacturing defect was found for the cartridge component, which could...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Monoject Standard Hypodermic Needle Recalled by Cardinal Health 200, LLC Due...
The Issue: Manufacturing defect was found for the cartridge component, which could...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Monoject" 201 Vet Pak Hypodermic Needle Recalled by Cardinal Health 200, LLC...
The Issue: Manufacturing defect was found for the cartridge component, which could...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Monoject Blunt Cannula Recalled by Cardinal Health 200, LLC Due to...
The Issue: Manufacturing defect was found for the cartridge component, which could...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Monoject Blunt Cannula Recalled by Cardinal Health 200, LLC Due to...
The Issue: Manufacturing defect was found for the cartridge component, which could...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Monoject Blunt Cannula Recalled by Cardinal Health 200, LLC Due to...
The Issue: Manufacturing defect was found for the cartridge component, which could...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Endotrac ECTR Hook/Triangle Blade Kit Recalled by Stryker GmbH Due to The...
The Issue: The seal integrity of the sterile bag containing the kits may be compromised.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Monoject 201 Vet Pak Hypodermic Needle Recalled by Cardinal Health 200, LLC...
The Issue: Manufacturing defect was found for the cartridge component, which could...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Monoject 201 Vet Pak Hypodermic Needle Recalled by Cardinal Health 200, LLC...
The Issue: Manufacturing defect was found for the cartridge component, which could...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Monoject 201 Vet Pak Hypodermic Needle Recalled by Cardinal Health 200, LLC...
The Issue: Manufacturing defect was found for the cartridge component, which could...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Losartan Potassium Tab. USP 50mg Recalled by Preferred Pharmaceuticals, Inc...
The Issue: CGMP Deviations: FDA lab confirmed presence of an impurity,...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Losartan Potassium 100 mg Recalled by Direct Rx Due to CGMP Deviations: FDA...
The Issue: CGMP Deviations: FDA lab confirmed presence of an impurity,...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Mycophenolate Mofetil for Injection Recalled by Par Pharmaceutical, Inc. Due...
The Issue: Presence of Particulate Matter; glass fragment observed in one vial of...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Ketorolac Tromethamine Injection Recalled by Sagent Pharmaceuticals Inc Due...
The Issue: Lack of Sterility Assurance: Microbial growth detected during a routine...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Relpax (eletriptan HBr) 40 mg Recalled by Pfizer Inc. Due to Labeling: Label...
The Issue: Labeling: Label Error on Declared Strength: an artwork error on the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Philips IntelliBridge System configured with a regional setting which uses...
The Issue: Infusion Pump Data Storage Accuracy-Data from the BBraun Space LAN or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MAHURKAR and Argyle acute hemodialysis catheters Recalled by COVIDIEN LLC...
The Issue: The priming volume values printed on the MAHURKA and Argyle acute catheters...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Patient Information Center iX configured with a regional setting...
The Issue: Infusion Pump Data Storage Accuracy-Data from the BBraun Space LAN or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips EPIQ and Affiniti Ultrasound Systems with software version 4.0:...
The Issue: There is a potential that the image of one patient could get unexpectedly...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DEXIS Titanium Intraoral Sensor Product Usage: The DEXIS Titanium Intraoral...
The Issue: The sensor's look up calibration files were incorrectly programmed during...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.