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. 2,748 recalls have been distributed to Georgia in the last 12 months.

53,623 total recalls
2,748 in last 12 months

Showing 1676116780 of 53,623 recalls

Medical DeviceApril 7, 2021· Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)

Recalled Item: Cobalt HF Quad MRI SureScan Implantable Cardioverter Defibrillators with...

The Issue: The device may contain a manufacturing defect of a missing resistance spot...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 7, 2021· Bard Access Systems Inc.

Recalled Item: Recalled by Bard Access Systems Inc. Due to Catheters contain two issues: 1....

The Issue: Catheters contain two issues: 1. the inner diameter of the distal connector...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 7, 2021· Bard Access Systems Inc.

Recalled Item: Recalled by Bard Access Systems Inc. Due to Catheters contain two issues: 1....

The Issue: Catheters contain two issues: 1. the inner diameter of the distal connector...

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

Class II — Potential Health HazardOngoing
DrugApril 6, 2021· Hyobin LLC

Recalled Item: PremierZen Black 5000 Recalled by Hyobin LLC Due to Marketed without...

The Issue: Marketed without Approved NDA/ANDA: FDA analysis results obtained the...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 6, 2021· Hyobin LLC

Recalled Item: Triple SupremeZen Plus 3500 Recalled by Hyobin LLC Due to Marketed without...

The Issue: Marketed without Approved NDA/ANDA: FDA analysis results obtained the...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 6, 2021· Hyobin LLC

Recalled Item: PremierZen Extreme 3000 Recalled by Hyobin LLC Due to Marketed without...

The Issue: Marketed without Approved NDA/ANDA: FDA analysis results obtained the...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceApril 6, 2021· Philips Respironics, Inc.

Recalled Item: BiPAP A40 System Silver Recalled by Philips Respironics, Inc. Due to Certain...

The Issue: Certain devices were built with motor assemblies that could contain...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 6, 2021· Philips Respironics, Inc.

Recalled Item: BiPAP A30 Recalled by Philips Respironics, Inc. Due to Certain devices were...

The Issue: Certain devices were built with motor assemblies that could contain...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 6, 2021· Philips Respironics, Inc.

Recalled Item: BiPAP A40 System Silver Recalled by Philips Respironics, Inc. Due to Certain...

The Issue: Certain devices were built with motor assemblies that could contain...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 6, 2021· Philips Respironics, Inc.

Recalled Item: BiPAP A40 Recalled by Philips Respironics, Inc. Due to Certain devices were...

The Issue: Certain devices were built with motor assemblies that could contain...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 6, 2021· Philips Respironics, Inc.

Recalled Item: BiPAP A40 Recalled by Philips Respironics, Inc. Due to Certain devices were...

The Issue: Certain devices were built with motor assemblies that could contain...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 6, 2021· Philips Respironics, Inc.

Recalled Item: BiPAP V30 Auto Recalled by Philips Respironics, Inc. Due to Certain devices...

The Issue: Certain devices were built with motor assemblies that could contain...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 6, 2021· LeMaitre Vascular, Inc.

Recalled Item: LeverEdge Contrast Injector: 35 cc syringe with ISO 594 female Recalled by...

The Issue: The firm received a complaint regarding particulate found in the packaging...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 5, 2021· W.L. Gore & Associates, Inc.

Recalled Item: GORE VIBIL Biliary Endoprosthesis: stents Recalled by W.L. Gore &...

The Issue: The Gore post market surveillance team received a complaint that a GORE¿...

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

Class II — Potential Health HazardOngoing
FoodApril 3, 2021· Hi Tech Pharmaceuticals

Recalled Item: ISOMORPH 28 PURE WHEY iSOLATE COOKIES N CREAM DIETARY SUPPLEMENT NET WT. 2lb...

The Issue: During an inspection by the FDA the firm was notified by FDA that the...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
FoodApril 3, 2021· Hi Tech Pharmaceuticals

Recalled Item: IFN iFORCE NUTRITION MASS GAINZ PROTEIN MATRIX BROWN SUGAR MAPLE Recalled by...

The Issue: During an inspection by the FDA the firm was notified by FDA that the...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
FoodApril 3, 2021· Hi Tech Pharmaceuticals

Recalled Item: ISOMORPH 28 PURE WHEY iSOLATE CHOCOLATE MILKSHAKE DIETARY SUPPLEMENT NET...

The Issue: During an inspection by the FDA the firm was notified by FDA that the...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
FoodApril 3, 2021· Hi Tech Pharmaceuticals

Recalled Item: ISOMORPH 28 PURE WHEY iSOLATE CHOCOLATE FUDGE POP DIETARY SUPPLEMENT...

The Issue: During an inspection by the FDA the firm was notified by FDA that the...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
FoodApril 3, 2021· Hi Tech Pharmaceuticals

Recalled Item: ISOMORPH 28 PURE WHEY iSOLATE BANANA CREAM PIE DIETARY SUPPLEMENT NET WT....

The Issue: During an inspection by the FDA the firm was notified by FDA that the...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
FoodApril 3, 2021· Hi Tech Pharmaceuticals

Recalled Item: ISOMORPH 28 PURE WHEY iSOLATE NEOPOLITAN ICE CREAM DIETARY SUPPLEMENT...

The Issue: During an inspection by the FDA the firm was notified by FDA that the...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund