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. 2,842 recalls have been distributed to Georgia in the last 12 months.

53,623 total recalls
2,842 in last 12 months

Showing 37813800 of 53,623 recalls

Medical DeviceDecember 12, 2024· Abiomed, Inc.

Recalled Item: Impella RP Flex with SmartAssist Recalled by Abiomed, Inc. Due to Optical...

The Issue: Optical Sensors have been damaged due to physical interaction between the...

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

Class I — Serious Health HazardOngoing
Medical DeviceDecember 12, 2024· Boston Scientific Corporation

Recalled Item: ESSENTIO DR Pacemaker Recalled by Boston Scientific Corporation Due to A...

The Issue: A subset of devices from the ACCOLADE Family of Pacemakers and CRT-Ps, built...

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

Class I — Serious Health HazardOngoing
Medical DeviceDecember 12, 2024· Boston Scientific Corporation

Recalled Item: VALITUDE CRT-P Recalled by Boston Scientific Corporation Due to A subset of...

The Issue: A subset of devices from the ACCOLADE Family of Pacemakers and CRT-Ps, built...

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

Class I — Serious Health HazardOngoing
Medical DeviceDecember 12, 2024· Boston Scientific Corporation

Recalled Item: ACCOLADE DR Pacemaker Recalled by Boston Scientific Corporation Due to A...

The Issue: A subset of devices from the ACCOLADE Family of Pacemakers and CRT-Ps, built...

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

Class I — Serious Health HazardOngoing
Medical DeviceDecember 12, 2024· Boston Scientific Corporation

Recalled Item: VISIONIST CRT-P Recalled by Boston Scientific Corporation Due to A subset of...

The Issue: A subset of devices from the ACCOLADE Family of Pacemakers and CRT-Ps, built...

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

Class I — Serious Health HazardOngoing
Medical DeviceDecember 12, 2024· Abiomed, Inc.

Recalled Item: Impella RP with SmartAssist Recalled by Abiomed, Inc. Due to Optical Sensors...

The Issue: Optical Sensors have been damaged due to physical interaction between the...

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

Class I — Serious Health HazardOngoing
Medical DeviceDecember 12, 2024· Boston Scientific Corporation

Recalled Item: ALTRUA 2 DR Pacemaker Recalled by Boston Scientific Corporation Due to A...

The Issue: A subset of devices from the ACCOLADE Family of Pacemakers and CRT-Ps, built...

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

Class I — Serious Health HazardOngoing
DrugDecember 11, 2024· Glenmark Pharmaceuticals Inc., USA

Recalled Item: chlorproMAZINE Hydrochloride Tablets Recalled by Glenmark Pharmaceuticals...

The Issue: CGMP Deviations: N-Nitroso-Desmethyl Chlorpromazine impurity (NNDCI) were...

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 11, 2024· Glenmark Pharmaceuticals Inc., USA

Recalled Item: chlorproMAZINE Hydrochloride Tablets Recalled by Glenmark Pharmaceuticals...

The Issue: CGMP Deviations: N-Nitroso-Desmethyl Chlorpromazine impurity (NNDCI) were...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceDecember 11, 2024· HF Acquisition Co LLC

Recalled Item: Biological Recalled by HF Acquisition Co LLC Due to Spore test strip...

The Issue: Spore test strip monitoring system, designed for routine monitoring of...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 11, 2024· Nuwellis Inc

Recalled Item: nuwellis AquaFlexFlow UF 500 Plus Recalled by Nuwellis Inc Due to The...

The Issue: The AquaFlexFlow UF 500 Plus extracorporeal blood circuit used with the...

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

Class I — Serious Health HazardOngoing
FoodDecember 10, 2024· Summit Import Corporation

Recalled Item: Yu Yee Recalled by Summit Import Corporation Due to Product tested and found...

The Issue: Product tested and found high levels of lead.

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

Class II — Potential Health HazardOngoing
Refund
FoodDecember 10, 2024· GARDNER'S CANDIES , INC

Recalled Item: Gardner's Candies Cappuccino Meltaway Bar 1.25 oz. (35g) Recalled by...

The Issue: Product contains Undeclared Allergen Tree Nuts (Cashews)

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

Class I — Serious Health HazardOngoing
Refund
DrugDecember 10, 2024· VIONA PHARMACEUTICALS INC

Recalled Item: Dapsone Gel 7.5% Recalled by VIONA PHARMACEUTICALS INC Due to Crystallization

The Issue: Crystallization

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 10, 2024· VIONA PHARMACEUTICALS INC

Recalled Item: Dapsone Gel 7.5% Recalled by VIONA PHARMACEUTICALS INC Due to Crystallization

The Issue: Crystallization

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 10, 2024· Regenerative Processing Plant, LLC

Recalled Item: LITE Regener-Eyes Recalled by Regenerative Processing Plant, LLC Due to Lack...

The Issue: Lack of Sterility Assurance

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 10, 2024· Regenerative Processing Plant, LLC

Recalled Item: PROFESSIONAL Regener-Eyes Recalled by Regenerative Processing Plant, LLC Due...

The Issue: Lack of Sterility Assurance

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceDecember 10, 2024· ev3 Inc

Recalled Item: Medtronic NanoCross Elite PTA catheter Recalled by ev3 Inc Due to There is...

The Issue: There is the potential for in-vivo balloon deflation issues, including...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 10, 2024· Mercury Enterprises, Inc. dba Mercury Medical

Recalled Item: Neo-Tee T-Piece Resuscitator Recalled by Mercury Enterprises, Inc. dba...

The Issue: Gas powered emergency resuscitator has a circuit flow controller...

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

Class I — Serious Health HazardOngoing
Medical DeviceDecember 10, 2024· Encore Medical, LP

Recalled Item: EMPOWR 3D Knee Tibial Insert Recalled by Encore Medical, LP Due to Knee...

The Issue: Knee insert package may contain an acetabular system, which may cause...

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

Class II — Potential Health HazardOngoing