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 34213440 of 54,363 recalls

FoodJanuary 24, 2025· Deiorio Foods Inc

Recalled Item: 5912MOD-CAU 11" Gluten Free Friendly Cauliflower Shell Recalled by Deiorio...

The Issue: Product may be contaminated with foreign objects (white fragments of...

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 24, 2025· SKY PACKAGING

Recalled Item: HydrALAZINE Hydrochloride Recalled by SKY PACKAGING Due to Failed...

The Issue: Failed Impurities/Degradation Specifications

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 24, 2025· SKY PACKAGING

Recalled Item: HydrALAZINE Hydrochloride Recalled by SKY PACKAGING Due to Failed...

The Issue: Failed Impurities/Degradation Specifications

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJanuary 24, 2025· Guangzhou Pluslife Biotech Co., Ltd.

Recalled Item: Brand Name: Pluslife SARS-CoV-2 Card Product Name: SARS-CoV-2 Nucleic Acid...

The Issue: Devices were distributed in the U.S. market without obtaining the required...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 24, 2025· Guangzhou Pluslife Biotech Co., Ltd.

Recalled Item: Brand Name: MiniDock Product Name: Integrated Nucleic Acid Testing Device...

The Issue: Devices were distributed in the U.S. market without obtaining the required...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 23, 2025· CareFusion 303, Inc.

Recalled Item: BD Alaris Pump Module The BD Alaris System Recalled by CareFusion 303, Inc....

The Issue: Due to User Manual/Direction for Use incorrectly instructing user to leave...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 23, 2025· CareFusion 303, Inc.

Recalled Item: BD Pyxis MedFlex 2.0 Bio-ID Spare Parts by CareFusion 303, Inc. Due to Due...

The Issue: Due to fingerprint scanner failing resulting in the scanner heating up.

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

Class II — Potential Health HazardOngoing
FoodJanuary 22, 2025· La Fiesta Food Products

Recalled Item: La Fiesta PAN RAYADO SAZONADO Bread Crumbs Seasoned Recalled by La Fiesta...

The Issue: Firm distributed a Seasoned Bread Crumb product with undeclared allergen...

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

Class I — Serious Health HazardOngoing
Refund
FoodJanuary 22, 2025· La Fiesta Food Products

Recalled Item: La Fiesta PAN RAYADO Bread Crumbs Recalled by La Fiesta Food Products Due to...

The Issue: Firm distributed a Bread Crumb product with undeclared allergen (Sesame) not...

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

Class I — Serious Health HazardOngoing
Refund
DrugJanuary 22, 2025· Glenmark Pharmaceuticals Inc., USA

Recalled Item: Carvedilol Tablets Recalled by Glenmark Pharmaceuticals Inc., USA Due to...

The Issue: CGMP Deviations:N-Nitroso Carvedilol I impurity (NNCI-I) were found to be...

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 22, 2025· Glenmark Pharmaceuticals Inc., USA

Recalled Item: Carvedilol Tablets Recalled by Glenmark Pharmaceuticals Inc., USA Due to...

The Issue: CGMP Deviations:N-Nitroso Carvedilol I impurity (NNCI-I) were found to be...

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 21, 2025· The Harvard Drug Group LLC dba Major Pharmaceuticals and Rugby Laboratories

Recalled Item: Lorazepam Tablets Recalled by The Harvard Drug Group LLC dba Major...

The Issue: Failed impurities/degradation specifications and Sub-potent Drug:...

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 21, 2025· Provepharm Inc.

Recalled Item: Phenylephrine HCl Injection Recalled by Provepharm Inc. Due to Presence of...

The Issue: Presence of Particulate Matter.

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

Class I — Serious Health HazardOngoing
Refund
DrugJanuary 21, 2025· The Harvard Drug Group LLC dba Major Pharmaceuticals and Rugby Laboratories

Recalled Item: Lorazepam Tablets Recalled by The Harvard Drug Group LLC dba Major...

The Issue: Failed impurities/degradation specifications and Sub-potent Drug:...

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 21, 2025· The Harvard Drug Group LLC dba Major Pharmaceuticals and Rugby Laboratories

Recalled Item: Lorazepam Tablets Recalled by The Harvard Drug Group LLC dba Major...

The Issue: Failed impurities/degradation specifications and Sub-potent Drug:...

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 21, 2025· AvKARE

Recalled Item: Irbesartan Tablets USP Recalled by AvKARE Due to Out of Specification for...

The Issue: Out of Specification for Dissolution

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJanuary 21, 2025· Tyber Medical

Recalled Item: A.L.P.S. mvX- ANATOMIC LAT FIB PLATE 12H RT- Anatomic Lateral Fibula Plate...

The Issue: Complaints of the locking screw passing through the locking hole...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 21, 2025· Tyber Medical

Recalled Item: A.L.P.S. mvX- MEDIAL TIBIA PLATE 16H RT -Medial Tibia Plate Recalled by...

The Issue: Complaints of the locking screw passing through the locking hole...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 21, 2025· Tyber Medical

Recalled Item: A.L.P.S. mvX-MEDIAL TIBIA PLATE 12H LT-Medial Tibia Plate Recalled by Tyber...

The Issue: Complaints of the locking screw passing through the locking hole...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 21, 2025· Tyber Medical

Recalled Item: A.L.P.S. mvX-MEDIAL TIBIA PLATE 6H LT-Medial Tibia Plate Recalled by Tyber...

The Issue: Complaints of the locking screw passing through the locking hole...

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

Class II — Potential Health HazardOngoing