Product Recalls in North Carolina

Product recalls affecting North Carolina — including food, drugs, consumer products, medical devices, and vehicles distributed to North Carolina. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,828 recalls have been distributed to North Carolina in the last 12 months.

54,363 total recalls
2,828 in last 12 months

Showing 30813100 of 54,363 recalls

Medical DeviceMarch 3, 2025· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Medline Convenience kits used for various procedures: 1) RHINOPLASTY PACK...

The Issue: There is a potential for open/weak seals on purchased breather pouches used...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 3, 2025· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: to RES Recalled by MEDLINE INDUSTRIES, LP - Northfield Due to There is a...

The Issue: There is a potential for open/weak seals on purchased breather pouches used...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 3, 2025· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Medline Convenience kits used for various procedures: 1) ANGIOGRAPHY DRAPE...

The Issue: There is a potential for open/weak seals on purchased breather pouches used...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 3, 2025· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Medline Convenience kits used for various procedures: 1) BASIC CATARACT...

The Issue: There is a potential for open/weak seals on purchased breather pouches used...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 3, 2025· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Medline Convenience kits used for various procedures: 1) PAIN PACK Recalled...

The Issue: There is a potential for open/weak seals on purchased breather pouches used...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 3, 2025· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Medline Convenience kits used for various procedures: 1) INTUBATION TRAY...

The Issue: There is a potential for open/weak seals on purchased breather pouches used...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 3, 2025· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Medline Convenience kits used for various procedures: 1) PRECIP TRAY...

The Issue: There is a potential for open/weak seals on purchased breather pouches used...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 3, 2025· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Medline Convenience kits used for various procedures: 1) DR. KHAN Recalled...

The Issue: There is a potential for open/weak seals on purchased breather pouches used...

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

Class II — Potential Health HazardOngoing
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· 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