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.

53,623 total recalls
2,661 in last 12 months

Showing 2390123920 of 53,623 recalls

DrugApril 22, 2019· Inopak Ltd

Recalled Item: INOFOAM Foaming E-2 Food Handling Wash with .6% PCMX Recalled by Inopak Ltd...

The Issue: CGMP Deviations: hand sanitizers and soaps were not produced under current...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugApril 22, 2019· Inopak Ltd

Recalled Item: INODERM Antiseptic Hand Soap (E-2) Recalled by Inopak Ltd Due to CGMP...

The Issue: CGMP Deviations: hand sanitizers and soaps were not produced under current...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugApril 22, 2019· Inopak Ltd

Recalled Item: Antibacterial Hand Soap Recalled by Inopak Ltd Due to CGMP Deviations: hand...

The Issue: CGMP Deviations: hand sanitizers and soaps were not produced under current...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugApril 22, 2019· Inopak Ltd

Recalled Item: Mild Health Care Antibacterial Hand Soap Recalled by Inopak Ltd Due to CGMP...

The Issue: CGMP Deviations: hand sanitizers and soaps were not produced under current...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugApril 22, 2019· Inopak Ltd

Recalled Item: Unison Hand Care Products Recalled by Inopak Ltd Due to CGMP Deviations:...

The Issue: CGMP Deviations: hand sanitizers and soaps were not produced under current...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugApril 22, 2019· Inopak Ltd

Recalled Item: AQUACIL instant foaming hand sanitizer Recalled by Inopak Ltd Due to CGMP...

The Issue: CGMP Deviations: hand sanitizers and soaps were not produced under current...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugApril 22, 2019· Inopak Ltd

Recalled Item: ANTIBACTERIAL Foaming Hand Wash With Moisturizers labeled as Antibacterial...

The Issue: CGMP Deviations: hand sanitizers and soaps were not produced under current...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugApril 22, 2019· Inopak Ltd

Recalled Item: Sani-Guard-SF Waterless Foam Hand Sanitizer Recalled by Inopak Ltd Due to...

The Issue: CGMP Deviations: hand sanitizers and soaps were not produced under current...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugApril 22, 2019· Inopak Ltd

Recalled Item: Instant Waterless Hand Sanitizer Recalled by Inopak Ltd Due to CGMP...

The Issue: CGMP Deviations: hand sanitizers and soaps were not produced under current...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceApril 22, 2019· Cook Inc.

Recalled Item: Cook Kwart Retro-Inject Ureteral Stent Set: PRODUCT/CATALOG NUMBER/GPN: 4.7...

The Issue: Kwart RetroInject Stent Set (Multi-Length) and Salle Intraoperative...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceApril 22, 2019· Cook Inc.

Recalled Item: Cook Salle Intraoperative Pyeloplasty Stent Set PRODUCT/CATALOG NUMBER/GPN:...

The Issue: Kwart RetroInject Stent Set (Multi-Length) and Salle Intraoperative...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceApril 19, 2019· Philips North America, LLC

Recalled Item: SureSigns VS3 NBP Recalled by Philips North America, LLC Due to System...

The Issue: System software inhibits the monitor and as a result does not measure,...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceApril 19, 2019· Philips North America, LLC

Recalled Item: SureSigns VS3 NBP Recalled by Philips North America, LLC Due to System...

The Issue: System software inhibits the monitor and as a result does not measure,...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceApril 19, 2019· Philips North America, LLC

Recalled Item: SureSigns VS4 NBP Recalled by Philips North America, LLC Due to System...

The Issue: System software inhibits the monitor and as a result does not measure,...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceApril 19, 2019· Philips North America, LLC

Recalled Item: SureSigns VS3 NBP Temp Recalled by Philips North America, LLC Due to System...

The Issue: System software inhibits the monitor and as a result does not measure,...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceApril 19, 2019· Philips North America, LLC

Recalled Item: SureSigns VS3 NBP Recalled by Philips North America, LLC Due to System...

The Issue: System software inhibits the monitor and as a result does not measure,...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceApril 19, 2019· Philips North America, LLC

Recalled Item: SureSigns VS3 NBP Recalled by Philips North America, LLC Due to System...

The Issue: System software inhibits the monitor and as a result does not measure,...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceApril 19, 2019· Philips North America, LLC

Recalled Item: SureSigns VS3 NBP Recalled by Philips North America, LLC Due to System...

The Issue: System software inhibits the monitor and as a result does not measure,...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceApril 19, 2019· Ethicon, Inc.

Recalled Item: ETHIBOND EXCEL ETHIBOND Polvester Suture-Green 75cm USP1 Single Armed CTX...

The Issue: Possibility that a suture raw material containing high endotoxin levels was...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceApril 19, 2019· Philips North America, LLC

Recalled Item: SureSigns VS4 Government Bundle Recalled by Philips North America, LLC Due...

The Issue: System software inhibits the monitor and as a result does not measure,...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing