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. 2,858 recalls have been distributed to Georgia in the last 12 months.

53,623 total recalls
2,858 in last 12 months

Showing 31213140 of 53,623 recalls

Medical DeviceMarch 3, 2025· Baxter Healthcare Corporation

Recalled Item: Baxter NovumIQ Syringe INFUSION SYSTEM Recalled by Baxter Healthcare...

The Issue: Baxter Healthcare Corporation is issuing an Urgent Medical Device Recall for...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 3, 2025· ZIMMER ORTHOPEDICS MANFACTURING LIMITED-GALWAY

Recalled Item: Comprehensive Shoulder Stem Recalled by ZIMMER ORTHOPEDICS MANFACTURING...

The Issue: Five complaints received where surgeon was unable to remove and/or connect...

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

Class II — Potential Health HazardOngoing
DrugFebruary 28, 2025· Glenmark Pharmaceuticals Inc., USA

Recalled Item: Carvedilol Tablets USP 25 mg Recalled by Glenmark Pharmaceuticals Inc., USA...

The Issue: CGMP Deviations; presence 'N-Nitroso Carvedilol I' Impurity above the...

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 28, 2025· Glenmark Pharmaceuticals Inc., USA

Recalled Item: Carvedilol Tablets USP 12.5 mg Recalled by Glenmark Pharmaceuticals Inc.,...

The Issue: CGMP Deviations; presence 'N-Nitroso Carvedilol I' Impurity above the...

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 28, 2025· Glenmark Pharmaceuticals Inc., USA

Recalled Item: Carvedilol Tablets USP 3.125mg Tablets a.)100-count bottle (NDC...

The Issue: CGMP Deviations; presence 'N-Nitroso Carvedilol I' Impurity above the...

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 28, 2025· Glenmark Pharmaceuticals Inc., USA

Recalled Item: Carvedilol Tablets USP 6.25 mg Recalled by Glenmark Pharmaceuticals Inc.,...

The Issue: CGMP Deviations; presence 'N-Nitroso Carvedilol I' Impurity above the...

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 28, 2025· Breckenridge Pharmaceutical, Inc.

Recalled Item: Duloxetine Delayed-Release Capsules Recalled by Breckenridge Pharmaceutical,...

The Issue: CGMP Deviations: Presence of N-nitroso-duloxetine impurity above FDA...

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 28, 2025· Breckenridge Pharmaceutical, Inc.

Recalled Item: Duloxetine Delayed-Release Capsules Recalled by Breckenridge Pharmaceutical,...

The Issue: CGMP Deviations: Presence of N-nitroso-duloxetine impurity above FDA...

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 28, 2025· Breckenridge Pharmaceutical, Inc.

Recalled Item: Duloxetine Delayed-Release Capsules Recalled by Breckenridge Pharmaceutical,...

The Issue: CGMP Deviations: Presence of N-nitroso-duloxetine impurity above FDA...

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 28, 2025· Sigan Industries Group Inc.

Recalled Item: Walgreens Recalled by Sigan Industries Group Inc. Due to Chemical...

The Issue: Chemical Contamination: Presence of benzene

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceFebruary 28, 2025· Stryker Spine

Recalled Item: Monterey AL Implant Inserter Recalled by Stryker Spine Due to Potential for...

The Issue: Potential for the gold unlock button to separate from the inserter.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 28, 2025· Reichert, Inc.

Recalled Item: Phoroptor VRx Digital System Model Numbers: 16241 Recalled by Reichert, Inc....

The Issue: The head of the phoropter head could come loose and potentially detach due...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 28, 2025· Reichert, Inc.

Recalled Item: Phoroptor VRx Digital System Model Numbers: 16242 Recalled by Reichert, Inc....

The Issue: The head of the phoropter head could come loose and potentially detach due...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 28, 2025· Stryker Spine

Recalled Item: Monterey AL Implant Inserter Recalled by Stryker Spine Due to Potential for...

The Issue: Potential for the gold unlock button to separate from the inserter.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 28, 2025· Stryker Spine

Recalled Item: Monterey AL Implant Inserter Recalled by Stryker Spine Due to Potential for...

The Issue: Potential for the gold unlock button to separate from the inserter.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 28, 2025· Stryker Spine

Recalled Item: Monterey AL Implant Inserter Recalled by Stryker Spine Due to Potential for...

The Issue: Potential for the gold unlock button to separate from the inserter.

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

Class II — Potential Health HazardOngoing
DrugFebruary 27, 2025· Amgen, Inc.

Recalled Item: Neupogen (filgrastim) For Injection Recalled by Amgen, Inc. Due to Stability...

The Issue: Stability data does not support expiry: the products have the potential to...

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 27, 2025· Amgen, Inc.

Recalled Item: Neupogen (filgrastim) For Injection Recalled by Amgen, Inc. Due to Stability...

The Issue: Stability data does not support expiry: the products have the potential to...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceFebruary 27, 2025· Premier Dental Products Co

Recalled Item: Premier Solo Diamond - Large Invented Cone Recalled by Premier Dental...

The Issue: The hardness not meeting the material specification and may cause the...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 27, 2025· Zimmer, Inc.

Recalled Item: NexGen LPS Flex Recalled by Zimmer, Inc. Due to The "Use with plate 7, 8, 9,...

The Issue: The "Use with plate 7, 8, 9, 10" compatibility statement on top of the label...

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

Class II — Potential Health HazardOngoing