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. 2,643 recalls have been distributed to Georgia in the last 12 months.

53,623 total recalls
2,643 in last 12 months

Showing 2836128380 of 53,623 recalls

FoodMarch 30, 2018· Nutrizone LLC

Recalled Item: Nirvanio Maeng Da Kratom all packages Recalled by Nutrizone LLC Due to...

The Issue: Dietary supplements have the potential to be contaminated with Salmonella.

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

Class I — Serious Health HazardOngoing
Refund
FoodMarch 30, 2018· Nutrizone LLC

Recalled Item: Cali Green Malay Kratom all packages Recalled by Nutrizone LLC Due to...

The Issue: Dietary supplements have the potential to be contaminated with Salmonella.

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

Class I — Serious Health HazardOngoing
Refund
FoodMarch 30, 2018· Nutrizone LLC

Recalled Item: Nirvanio Special Reserve Kratom all packages Recalled by Nutrizone LLC Due...

The Issue: Dietary supplements have the potential to be contaminated with Salmonella.

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

Class I — Serious Health HazardOngoing
Refund
FoodMarch 30, 2018· Nutrizone LLC

Recalled Item: Cali Maeng Da Kratom all packages Recalled by Nutrizone LLC Due to Potential...

The Issue: Dietary supplements have the potential to be contaminated with Salmonella.

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

Class I — Serious Health HazardOngoing
Refund
FoodMarch 30, 2018· Nutrizone LLC

Recalled Item: Pain Out Thai Kratom all packages Recalled by Nutrizone LLC Due to Potential...

The Issue: Dietary supplements have the potential to be contaminated with Salmonella.

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceMarch 30, 2018· GE Medical Systems, LLC

Recalled Item: MR Surgical Suite Option Product The MR Surgical Option when Recalled by GE...

The Issue: There is a potential safety issue with the table transfer release of the MR...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 30, 2018· PENTAX of America Inc

Recalled Item: C2 CryoBalloon Focal Catheter Recalled by PENTAX of America Inc Due to The...

The Issue: The catheter alignment arrow printed onto the strain relief is not aligned...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 30, 2018· Edwards Lifesciences, LLC

Recalled Item: Edwards Lifesciences' IntraClude Intra-Aortic Occlusion Device. Packaged in...

The Issue: Possible leak at distal open end of the strain relief, which causes medical...

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

Class II — Potential Health HazardOngoing
DrugMarch 29, 2018· United Pacific Co Ltd

Recalled Item: Zhong Hua Jiu (menthol 1%) Patch Recalled by United Pacific Co Ltd Due to...

The Issue: CGMP Deviations: the product was produced with substandard GMP manufacturing...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 29, 2018· Akorn, Inc.

Recalled Item: 24-HOUR Oral Care q2 Kit with Ballard* Technology Recalled by Akorn, Inc....

The Issue: Subpotent Drug: Product crystallization with accompanying low out of...

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

Class III — Low RiskOngoing
Refund
DrugMarch 29, 2018· Akorn, Inc.

Recalled Item: 24-HOUR Oral Care q4 Kit with Ballard* Technology Recalled by Akorn, Inc....

The Issue: Subpotent Drug: Product crystallization with accompanying low out of...

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

Class III — Low RiskOngoing
Refund
DrugMarch 29, 2018· Akorn, Inc.

Recalled Item: Chlorhexidine Gluconate Oral Rinse Recalled by Akorn, Inc. Due to Subpotent...

The Issue: Subpotent Drug: Product crystallization with accompanying low out of...

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

Class III — Low RiskOngoing
Refund
FoodMarch 29, 2018· purely elizabeth.

Recalled Item: Chocolate Sea Salt Probiotic Granola Recalled by purely elizabeth. Due to...

The Issue: Chocolate Sea Salt Probiotic Granola due to undeclared soy lecithin.

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMarch 29, 2018· GE Medical Systems, SCS

Recalled Item: Innova IGS 630/520/530/540 Interventional Fluoroscopic X-ray Systems...

The Issue: The Discovery IGS and Innova IGS systems may experience X-ray abort errors...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 29, 2018· GE Medical Systems, SCS

Recalled Item: Discovery IGS 730 Interventional Fluoroscopic X-ray Systems Recalled by GE...

The Issue: The Discovery IGS and Innova IGS systems may experience X-ray abort errors...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 29, 2018· Stryker Sustainability Solutions

Recalled Item: Coronary Sinus (CS) Uni-Directional Diagnostic Electrophysiology (EP)...

The Issue: Thrombogenicity test results demonstrated that both the test devices (SSS)...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 29, 2018· GE Medical Systems, SCS

Recalled Item: Discovery IGS 740 Interventional Fluoroscopic X-ray Systems Recalled by GE...

The Issue: The Discovery IGS and Innova IGS systems may experience X-ray abort errors...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 29, 2018· Beckman Coulter Inc.

Recalled Item: iChem VELOCITY Automated Urine Chemistry System Recalled by Beckman Coulter...

The Issue: The Strip Provider Modules (SPM) on some of the instruments had not been...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 29, 2018· Cook Inc.

Recalled Item: Connecting Tube - Female to Male Luer Lock Recalled by Cook Inc. Due to...

The Issue: Cap-adapter assembly of the device may potentially not be adequately...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 29, 2018· Cook Inc.

Recalled Item: Connecting Tube - Female to Male Luer Lock Recalled by Cook Inc. Due to...

The Issue: Cap-adapter assembly of the device may potentially not be adequately...

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

Class II — Potential Health HazardOngoing