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 33213340 of 54,363 recalls

Medical DeviceFebruary 6, 2025· American Contract Systems Inc

Recalled Item: MAJOR DIEP Recalled by American Contract Systems Inc Due to ACS is unable to...

The Issue: ACS is unable to confirm product sterilization assurance requirements were...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 6, 2025· American Contract Systems Inc

Recalled Item: LAPAROSCOPY PACK Recalled by American Contract Systems Inc Due to ACS is...

The Issue: ACS is unable to confirm product sterilization assurance requirements were...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 6, 2025· American Contract Systems Inc

Recalled Item: SPINE LUMBAR PACK Recalled by American Contract Systems Inc Due to ACS is...

The Issue: ACS is unable to confirm product sterilization assurance requirements were...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 6, 2025· American Contract Systems Inc

Recalled Item: EAR PACK Recalled by American Contract Systems Inc Due to ACS is unable to...

The Issue: ACS is unable to confirm product sterilization assurance requirements were...

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

Class II — Potential Health HazardOngoing
DrugFebruary 6, 2025· SUN PHARMACEUTICAL INDUSTRIES INC

Recalled Item: Morphine Sulfate Extended-Release Tablets Recalled by SUN PHARMACEUTICAL...

The Issue: Failed Dissolution Specifications

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 6, 2025· Padagis US LLC

Recalled Item: Estradiol Gel Recalled by Padagis US LLC Due to Defective Container: Some...

The Issue: Defective Container: Some packets may not be fully sealed, potentially...

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

Class II — Potential Health HazardOngoing
Refund
FoodFebruary 5, 2025· FEEL GOOD FOODS INC

Recalled Item: Feel Good Foods Recalled by FEEL GOOD FOODS INC Due to Foreign Object...

The Issue: Foreign object (metal pieces).

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceFebruary 5, 2025· Baxter Healthcare Corporation

Recalled Item: Baxter Sigma Spectrum Infusion System (V6 Platform) Recalled by Baxter...

The Issue: There is the potential for missing motor mounting screws, which may have...

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

Class I — Serious Health HazardOngoing
Medical DeviceFebruary 5, 2025· Baxter Healthcare Corporation

Recalled Item: Baxter Spectrum IQ Infusion System with Dose IQ Safety Software Recalled by...

The Issue: There is the potential for missing motor mounting screws, which may have...

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

Class I — Serious Health HazardOngoing
Medical DeviceFebruary 5, 2025· Bard Peripheral Vascular Inc

Recalled Item: Rotarex Atherectomy System and Instructions for Use Recalled by Bard...

The Issue: Atherectomy Catheter eIFU updated to clarify and emphasize procedural steps...

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

Class I — Serious Health HazardOngoing
Medical DeviceFebruary 5, 2025· Beckman Coulter, Inc.

Recalled Item: Access 2 Immunoassay Analyzer Recalled by Beckman Coulter, Inc. Due to...

The Issue: Beckman Coulter identified that an issue for Access 2 Sample Motors (B48016)...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 5, 2025· Medtronic Perfusion Systems

Recalled Item: Aortic Root Cannula: 1. DLP Aortic Root Cannula A. CANNULA Recalled by...

The Issue: Unexpected loose material in the male luer used in the aortic root cannula...

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

Class I — Serious Health HazardOngoing
Medical DeviceFebruary 5, 2025· Beckman Coulter, Inc.

Recalled Item: DxI 9000 Access Immunoassay Analyzer Recalled by Beckman Coulter, Inc. Due...

The Issue: the DxI 9000 encoder wheel was misaligned on the motor shaft, leading to...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 5, 2025· INTELERAD MEDICAL SYSTEMS INCORPORATED

Recalled Item: IntelePACS (Image Fusion Module) - InteleViewer Recalled by INTELERAD...

The Issue: A software application that receives digital images and data from various...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 5, 2025· Medical Information Technology, Inc.

Recalled Item: MEDITECH Expanse Laboratory (LAB) Recalled by Medical Information...

The Issue: Entering multiple keys that trigger input simultaneously may remove data...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 4, 2025· Angiodynamics, Inc.

Recalled Item: IsoLoc Short Profile Prostate Immobilization Treatment Balloon Device Kit...

The Issue: Product is mislabeled with the incorrect fill volume.

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

Class II — Potential Health HazardOngoing
DrugFebruary 4, 2025· AvKARE

Recalled Item: Silodosin Capsules Recalled by AvKARE Due to Subpotent Drug: Out of...

The Issue: Subpotent Drug: Out of Specification (OOS) result for De hydro Impurity...

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

Class II — Potential Health HazardOngoing
Refund
FoodFebruary 4, 2025· Chicken of the Sea; Thai Union

Recalled Item: Trader Joe's branded Solid Light Yellowfin Tuna in olive oil Recalled by...

The Issue: Product's easy-pull lid was not secured properly and may cause the product...

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

Class II — Potential Health HazardOngoing
Refund
FoodFebruary 4, 2025· Chicken of the Sea; Thai Union

Recalled Item: Trader Joe's branded Solid White Albacore Tuna in water Recalled by Chicken...

The Issue: Product's easy-pull lid was not secured properly and may cause the product...

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

Class II — Potential Health HazardOngoing
Refund
FoodFebruary 4, 2025· Chicken of the Sea; Thai Union

Recalled Item: Trader Joe's branded Solid White Albacore Tuna in Water Recalled by Chicken...

The Issue: Product's easy-pull lid was not secured properly and may cause the product...

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

Class II — Potential Health HazardOngoing
Refund