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. 2,863 recalls have been distributed to Georgia in the last 12 months.

53,623 total recalls
2,863 in last 12 months

Showing 4160 of 53,623 recalls

Medical DeviceFebruary 2, 2026· B Braun Medical Inc

Recalled Item: Brand Name: B. Braun Product Name: 21GA WINGED INFUSION Recalled by B Braun...

The Issue: The potential for the needle tip to be dull/blunt, difficult to advance,...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 30, 2026· Covidien LLC

Recalled Item: HealthCast "Vital Sync" Remote Patient Monitoring System which consists of:...

The Issue: Due to complaints and investigations stating that alarms from the primary...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 30, 2026· Medline Industries, LP

Recalled Item: Medline Kits containing Cardinal Health s Aqua-Seal Chest Drainage Unit:...

The Issue: The instructions for use (IFUs) on specified Cardinal Health Chest Drainage...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 30, 2026· Beckman Coulter Mishima K.K.

Recalled Item: CHEMISTRY ANALYZER AU5800 Recalled by Beckman Coulter Mishima K.K. Due to A...

The Issue: A delay in results may occur. When clinical chemistry analyzer calibration...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 30, 2026· Beckman Coulter Mishima K.K.

Recalled Item: DxC 700 AU Recalled by Beckman Coulter Mishima K.K. Due to A delay in...

The Issue: A delay in results may occur. When clinical chemistry analyzer calibration...

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

Class II — Potential Health HazardOngoing
DrugJanuary 29, 2026· Teva Pharmaceuticals USA, Inc

Recalled Item: Metoprolol Succinate Extended-Release Tablets Recalled by Teva...

The Issue: Failed Dissolution Specifications

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJanuary 29, 2026· Olympus Corporation of the Americas

Recalled Item: Olympus Single Use Biopsy Valve. Model/Catalog Number: MAJ-1218. 20 units...

The Issue: Potential for rubber fragment detachment during use.

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 29, 2026· Olympus Corporation of the Americas

Recalled Item: Olympus Single use Biopsy Valve. Model/Catalog Number: MAJ-210. 20 units...

The Issue: Potential for rubber fragment detachment during use.

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

Class II — Potential Health HazardOngoing
DrugJanuary 29, 2026· Teva Pharmaceuticals USA, Inc

Recalled Item: Metoprolol Succinate Extended-Release Tablets Recalled by Teva...

The Issue: Failed Dissolution Specifications

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 29, 2026· Teva Pharmaceuticals USA, Inc

Recalled Item: Metoprolol Succinate Extended-Release Tablets Recalled by Teva...

The Issue: Failed Dissolution Specifications

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 29, 2026· Teva Pharmaceuticals USA, Inc

Recalled Item: Metoprolol Succinate Extended-Release Tablets Recalled by Teva...

The Issue: Failed Dissolution Specifications

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

Class II — Potential Health HazardOngoing
Refund
FoodJanuary 28, 2026· MIN JIANG FOOD STORE INC DBA KOI KOI TRADING

Recalled Item: Fish Ball Recalled by MIN JIANG FOOD STORE INC DBA KOI KOI TRADING Due to...

The Issue: Undeclared allergen ingredient (Wheat and Sesame)

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

Class I — Serious Health HazardOngoing
Refund
FoodJanuary 28, 2026· MIN JIANG FOOD STORE INC DBA KOI KOI TRADING

Recalled Item: Fish Ball Recalled by MIN JIANG FOOD STORE INC DBA KOI KOI TRADING Due to...

The Issue: Undeclared allergen ingredient (Wheat and Sesame)

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceJanuary 28, 2026· Medline Industries, LP

Recalled Item: Medline Medcrest Surgical Gowns: MDTGXC4J5XL DBQ-GOWN Recalled by Medline...

The Issue: Fabric may experience premature delamination when using included laundering...

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

Class II — Potential Health HazardOngoing
FoodJanuary 28, 2026· Art Monkey LLC dba Why Not Natural

Recalled Item: Why Not Natural Moringa Capsules 120 capsule bottle marked with Recalled by...

The Issue: 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 DeviceJanuary 28, 2026· Medline Industries, LP

Recalled Item: Medline Surgical Drapes: MDTBTCS6070GN DBD-DRAPE Recalled by Medline...

The Issue: Fabric may experience premature delamination when using included laundering...

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

Class II — Potential Health HazardOngoing
FoodJanuary 28, 2026· MIN JIANG FOOD STORE INC DBA KOI KOI TRADING

Recalled Item: Fish Ball Recalled by MIN JIANG FOOD STORE INC DBA KOI KOI TRADING Due to...

The Issue: Undeclared allergen ingredient (Wheat and Sesame)

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceJanuary 27, 2026· Abiomed, Inc.

Recalled Item: Impella RP with SmartAssist. Product Code: 0046-0035. Recalled by Abiomed,...

The Issue: Differential pressure (dP) sensor in Impella RP devices may malfunction,...

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

Class I — Serious Health HazardOngoing
Medical DeviceJanuary 27, 2026· Abiomed, Inc.

Recalled Item: Impella RP Flex with SmartAssist. Product Code: 1000323. Recalled by...

The Issue: Differential pressure (dP) sensor in Impella RP devices may malfunction,...

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

Class I — Serious Health HazardOngoing
Medical DeviceJanuary 27, 2026· Abiomed, Inc.

Recalled Item: Impella RP. Product Code: 0046-0011. Recalled by Abiomed, Inc. Due to...

The Issue: Differential pressure (dP) sensor in Impella RP devices may malfunction,...

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

Class I — Serious Health HazardOngoing