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. 2,793 recalls have been distributed to Georgia in the last 12 months.
Showing 11781–11800 of 53,623 recalls
Recalled Item: Starling Monitor Recalled by Baxter Healthcare Corporation Due to Labeling...
The Issue: Labeling has incorrect or incomplete Unique Device Identification (UDI)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synergy Hand Sanitizer Recalled by SUPERIOR GLOVE WORKS, LTD. Due to CGMP...
The Issue: CGMP Deviations: FDA analysis found product to contain acetaldehyde impurity...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Recreo Hair Growth Laser Comb Recalled by OMM Imports, Inc. dba Zero Gravity...
The Issue: The firm distributed the laser products without affixing the warning,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Disposable Surgical Level 3 Gown Recalled by Texas Medical Technology Inc....
The Issue: Surgical gowns recalled due to gown fabric failing to pass the hydrostatic...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Introcan Safety FEP 14G Recalled by B Braun Medical Inc Due to Potential for...
The Issue: Potential for leakage at the catheter hub.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Veritas Advanced Infusion Packs. Used in ophthalmic procedures. Recalled by...
The Issue: As a result of returned product complaints for Veritas Phaco packs related...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Lidocaine Hydrochloride Jelly USP Recalled by Akorn, Inc. Due to cGMP...
The Issue: cGMP Deviations: Turbidity discovered in Artificial Tears Ointment during...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Sodium Chloride Ophthalmic Ointment USP Recalled by Akorn, Inc. Due to cGMP...
The Issue: cGMP Deviations: Turbidity discovered in Artificial Tears Ointment during...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: FULL VISION INC. TRACKMASTER Recalled by Full Vision Inc Due to This has...
The Issue: This has been identified a rare occurrence, under a specific scenario, where...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FULL VISION INC. TRACKMASTER Recalled by Full Vision Inc Due to This has...
The Issue: This has been identified a rare occurrence, under a specific scenario, where...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FULL VISION INC. TRACKMASTER Recalled by Full Vision Inc Due to This has...
The Issue: This has been identified a rare occurrence, under a specific scenario, where...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FULL VISION INC. TRACKMASTER Recalled by Full Vision Inc Due to This has...
The Issue: This has been identified a rare occurrence, under a specific scenario, where...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FULL VISION INC. TRACKMASTER Recalled by Full Vision Inc Due to This has...
The Issue: This has been identified a rare occurrence, under a specific scenario, where...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FULL VISION INC. TRACKMASTER Recalled by Full Vision Inc Due to This has...
The Issue: This has been identified a rare occurrence, under a specific scenario, where...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FULL VISION INC. TRACKMASTER Recalled by Full Vision Inc Due to This has...
The Issue: This has been identified a rare occurrence, under a specific scenario, where...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MICRO-X ROVER MOBILE X-RAY SYSTEM Recalled by Micro-X Ltd. Due to Software...
The Issue: Software calibration error with product equip with a Dose Area Product (DAP)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The product is a handheld ultraviolet-C germicidal wand and contains...
The Issue: Excessive ultraviolet-C radiation
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: N Antiserum to Human IgG Recalled by SIEMENS HEALTHCARE DIAGNOSTICS INC Due...
The Issue: N Antiserum to Human IgG are not meeting the current High-Dose Hook Effect...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: N Antiserum to Human IgG Recalled by SIEMENS HEALTHCARE DIAGNOSTICS INC Due...
The Issue: N Antiserum to Human IgG are not meeting the current High-Dose Hook Effect...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hammertoe Continuous Compression Implant (CCI) Kit Part Number: 46.239.001...
The Issue: Drill Pin (drill bit) is not compatible with the Drill Template included in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.