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 28412860 of 54,363 recalls

Medical DeviceMarch 27, 2025· Bausch & Lomb Surgical, Inc.

Recalled Item: Intraocular lens. enVista Monofocal IOL Recalled by Bausch & Lomb Surgical,...

The Issue: In response to an increased number of reports of toxic anterior segment...

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 27, 2025· Galt Medical Corporation

Recalled Item: GALT Centeze Catheter DRC-002-06 The Centeze is intended Recalled by Galt...

The Issue: Due to a potential open seal in the sterile barrier packaging .

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 27, 2025· IHB OPERATIONS B.V.

Recalled Item: Skytron Freedom 4FXS-60 Heavy Duty Monitor Mount Recalled by IHB OPERATIONS...

The Issue: The mounting hardware that is supplied with the 4FXS-60 monitor bracket does...

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

Class II — Potential Health HazardOngoing
FoodMarch 26, 2025· The Truck Farm, LLC

Recalled Item: Desert Farms Jalapeno Mustard. Caution to after opening. The Recalled by The...

The Issue: The product is in violation for not having an approved filed process and for...

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

Class II — Potential Health HazardOngoing
Refund
FoodMarch 26, 2025· Frito-Lay, Inc. Headquarters

Recalled Item: Tostitos Cantina Traditional Yellow Corn Tortilla Chips. Net Wt. 13oz....

The Issue: Undeclared allergen (milk).

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

Class I — Serious Health HazardOngoing
Refund
DrugMarch 26, 2025· Chattem Inc

Recalled Item: Unisom Recalled by Chattem Inc Due to CGMP Deviations; detection of...

The Issue: CGMP Deviations; detection of Nitrosamine Drug Substance-Related Impurities...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 26, 2025· Breckenridge Pharmaceutical, Inc.

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

The Issue: CGMP Deviations: presence of Nitrosamine Drug Substance Related Impurity...

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

Class II — Potential Health HazardOngoing
Refund
FoodMarch 25, 2025· MTN OPS, LLC

Recalled Item: MTN OPS MULTI-V Men's Daily Multivitamin dietary supplement Recalled by MTN...

The Issue: Undeclared soy flour

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMarch 25, 2025· Conformis Inc.

Recalled Item: restor3d Cordera Hip System. ACETABULAR LINER GRP C 36MM LIP. Recalled by...

The Issue: The hip cup liner that was packaged with the incorrect labeling....

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

Class II — Potential Health HazardOngoing
DrugMarch 24, 2025· Amerisource Health Services LLC

Recalled Item: Voriconazole Tablets Recalled by Amerisource Health Services LLC Due to cGMP...

The Issue: cGMP Deviations: Received notification from their supplier requesting they...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMarch 24, 2025· PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

Recalled Item: Intera 1.5T Explorer/Nova Dual Recalled by PHILIPS MEDICAL SYSTEMS NEDERLAND...

The Issue: The Quadrature Body Coil (QBC) seal adhesive may fail, creating sharp edges...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 24, 2025· PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

Recalled Item: Intera 1.5T Master/Nova Recalled by PHILIPS MEDICAL SYSTEMS NEDERLAND B.V....

The Issue: The Quadrature Body Coil (QBC) seal adhesive may fail, creating sharp edges...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 24, 2025· PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

Recalled Item: SmartPath to dStream for 3.0T Recalled by PHILIPS MEDICAL SYSTEMS NEDERLAND...

The Issue: The Quadrature Body Coil (QBC) seal adhesive may fail, creating sharp edges...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 24, 2025· PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

Recalled Item: SmartPath to dStream for 1.5T Recalled by PHILIPS MEDICAL SYSTEMS NEDERLAND...

The Issue: The Quadrature Body Coil (QBC) seal adhesive may fail, creating sharp edges...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 24, 2025· PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

Recalled Item: Intera 1.0T Omni/Stellar Recalled by PHILIPS MEDICAL SYSTEMS NEDERLAND B.V....

The Issue: The Quadrature Body Coil (QBC) seal adhesive may fail, creating sharp edges...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 24, 2025· PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

Recalled Item: Enterprise 1.5T Recalled by PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. Due to...

The Issue: The Quadrature Body Coil (QBC) seal adhesive may fail, creating sharp edges...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 24, 2025· PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

Recalled Item: Intera 1.5T Omni/Stellar Recalled by PHILIPS MEDICAL SYSTEMS NEDERLAND B.V....

The Issue: The Quadrature Body Coil (QBC) seal adhesive may fail, creating sharp edges...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 24, 2025· PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

Recalled Item: Intera 0.5T Standard Recalled by PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. Due...

The Issue: The Quadrature Body Coil (QBC) seal adhesive may fail, creating sharp edges...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 24, 2025· PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

Recalled Item: Intera 3.0T Quasar Dual Recalled by PHILIPS MEDICAL SYSTEMS NEDERLAND B.V....

The Issue: The Quadrature Body Coil (QBC) seal adhesive may fail, creating sharp edges...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 24, 2025· PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

Recalled Item: Intera 1.5T Power/Pulsar Recalled by PHILIPS MEDICAL SYSTEMS NEDERLAND B.V....

The Issue: The Quadrature Body Coil (QBC) seal adhesive may fail, creating sharp edges...

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

Class II — Potential Health HazardOngoing