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. 2,859 recalls have been distributed to Georgia in the last 12 months.

53,623 total recalls
2,859 in last 12 months

Showing 701720 of 53,623 recalls

Medical DeviceNovember 14, 2025· Olympus Corporation of the Americas

Recalled Item: Brand Name: ShockPulse-SE Lithotripsy System SPL-SR Product Name:...

The Issue: Ongoing investigations identified additional instances of the device...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 14, 2025· Olympus Corporation of the Americas

Recalled Item: Brand Name: ShockPulse-SE Lithotripsy System SPL-S Product Name:...

The Issue: Ongoing investigations identified additional instances of the device...

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

Class II — Potential Health HazardOngoing
DrugNovember 14, 2025· Cipla USA, Inc.

Recalled Item: Cinacalcet Hydrochloride Tablets Recalled by Cipla USA, Inc. Due to CGMP...

The Issue: CGMP Deviations: the presence of a nitrosamine impurity,...

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 14, 2025· Cipla USA, Inc.

Recalled Item: Cinacalcet Hydrochloride Tablets Recalled by Cipla USA, Inc. Due to CGMP...

The Issue: CGMP Deviations: the presence of a nitrosamine impurity,...

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 14, 2025· Cipla USA, Inc.

Recalled Item: Cinacalcet Hydrochloride Tablets Recalled by Cipla USA, Inc. Due to CGMP...

The Issue: CGMP Deviations: the presence of a nitrosamine impurity,...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceNovember 14, 2025· AVID Medical, Inc.

Recalled Item: Halyard Recalled by AVID Medical, Inc. Due to Potential for incomplete seal...

The Issue: Potential for incomplete seal on header bag.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 14, 2025· AVID Medical, Inc.

Recalled Item: Halyard Recalled by AVID Medical, Inc. Due to Potential for incomplete seal...

The Issue: Potential for incomplete seal on header bag.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 14, 2025· GE Medical Systems China Co., Ltd.

Recalled Item: GE Healthcare Carestation anesthesia system Recalled by GE Medical Systems...

The Issue: Potential unexpected shutdown of Carestation 600 and 700 Series Anesthesia...

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

Class I — Serious Health HazardOngoing
Medical DeviceNovember 14, 2025· AVID Medical, Inc.

Recalled Item: Halyard Recalled by AVID Medical, Inc. Due to Potential for incomplete seal...

The Issue: Potential for incomplete seal on header bag.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 14, 2025· AVID Medical, Inc.

Recalled Item: Halyard Recalled by AVID Medical, Inc. Due to Potential for incomplete seal...

The Issue: Potential for incomplete seal on header bag.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 14, 2025· Fresenius Kabi USA, LLC

Recalled Item: Ivenix Infusion System (IIS) Recalled by Fresenius Kabi USA, LLC Due to...

The Issue: Software version 5.10.1 and earlier contain anomalies that have the...

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

Class I — Serious Health HazardOngoing
Medical DeviceNovember 14, 2025· GE Medical Systems China Co., Ltd.

Recalled Item: GE Healthcare Carestation anesthesia system Recalled by GE Medical Systems...

The Issue: Potential unexpected shutdown of Carestation 600 and 700 Series Anesthesia...

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

Class I — Serious Health HazardOngoing
Medical DeviceNovember 14, 2025· AVID Medical, Inc.

Recalled Item: Halyard Recalled by AVID Medical, Inc. Due to Potential for incomplete seal...

The Issue: Potential for incomplete seal on header bag.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 14, 2025· GE Medical Systems China Co., Ltd.

Recalled Item: GE Healthcare Carestation anesthesia system Power Management Board (PMB)...

The Issue: Potential unexpected shutdown of Carestation 600 and 700 Series Anesthesia...

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

Class I — Serious Health HazardOngoing
FoodNovember 13, 2025· Jeni's Splendid Ice Creams LLC

Recalled Item: Jeni's Passion Fruit Dreamsicle Ice Cream Bars Recalled by Jeni's Splendid...

The Issue: Undeclared allergens - wheat and soy

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceNovember 13, 2025· Abbott Laboratories

Recalled Item: Alinity ci-series System Control Module (SCM) Recalled by Abbott...

The Issue: Abbott Laboratories is recalling their Alinity ci-series System Control...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 13, 2025· Medtronic MiniMed, Inc.

Recalled Item: InPen App Recalled by Medtronic MiniMed, Inc. Due to When app is uninstalled...

The Issue: When app is uninstalled and reinstalled, insulin pen software issue causes...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 13, 2025· Medline Industries, LP

Recalled Item: SCISSORS Recalled by Medline Industries, LP Due to The items may have weak...

The Issue: The items may have weak packaging seals that may result in a breach of...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 13, 2025· Medline Industries, LP

Recalled Item: FORCEP Recalled by Medline Industries, LP Due to The items may have weak...

The Issue: The items may have weak packaging seals that may result in a breach of...

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

Class II — Potential Health HazardOngoing
FoodNovember 12, 2025· Genepro Protein, Inc.

Recalled Item: Genepro Whey 4th Generation Plasma Treated Protein Recalled by Genepro...

The Issue: Product is mislabeled - the labeling contains incorrect ingredient...

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

Class I — Serious Health HazardOngoing
Refund