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. 1,913 recalls have been distributed to North Carolina in the last 12 months.

54,363 total recalls
1,913 in last 12 months

Showing 2566125680 of 54,363 recalls

FoodNovember 1, 2018· Sysco Charlotte

Recalled Item: Quality Crab CRAB MEAT LUMP NC Recalled by Sysco Charlotte Due to The firm...

The Issue: The firm discovered that one of their coolers malfunctioned and the food was...

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

Class II — Potential Health HazardOngoing
Refund
FoodNovember 1, 2018· Sysco Charlotte

Recalled Item: SMITHFIELD CHEESE CREAM Recalled by Sysco Charlotte Due to The firm...

The Issue: The firm discovered that one of their coolers malfunctioned and the food was...

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

Class II — Potential Health HazardOngoing
Refund
FoodNovember 1, 2018· Sysco Charlotte

Recalled Item: GFGB SAUCE TARTAR Recalled by Sysco Charlotte Due to The firm discovered...

The Issue: The firm discovered that one of their coolers malfunctioned and the food was...

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

Class II — Potential Health HazardOngoing
Refund
FoodNovember 1, 2018· Sysco Charlotte

Recalled Item: Packer KALE FRESH LACINATO-TUSCAN¿ Recalled by Sysco Charlotte Due to The...

The Issue: The firm discovered that one of their coolers malfunctioned and the food was...

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

Class II — Potential Health HazardOngoing
Refund
FoodNovember 1, 2018· Sysco Charlotte

Recalled Item: Packer Arugula Baby Organic Recalled by Sysco Charlotte Due to The firm...

The Issue: The firm discovered that one of their coolers malfunctioned and the food was...

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

Class II — Potential Health HazardOngoing
Refund
FoodNovember 1, 2018· Sysco Charlotte

Recalled Item: Pacific Harbor CRAB MEAT HAANII JMBO LUMP CHN Recalled by Sysco Charlotte...

The Issue: The firm discovered that one of their coolers malfunctioned and the food was...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceNovember 1, 2018· LivaNova USA Inc.

Recalled Item: SORIN Heater-Cooler System 3T 120V~/60Hz Description of product: Recalled by...

The Issue: The firm has become aware that due to a chemical reaction, the...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 1, 2018· ORTHO-CLINICAL DIAGNOSTICS

Recalled Item: VITROS NT-proBNP Reagent Recalled by ORTHO-CLINICAL DIAGNOSTICS Due to The...

The Issue: The firm is extending their previous July 2018 recall to include additional...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 1, 2018· ORTHO-CLINICAL DIAGNOSTICS

Recalled Item: VITROS Anti-HBe Reagent Pack Recalled by ORTHO-CLINICAL DIAGNOSTICS Due to...

The Issue: The firm is extending their previous July 2018 recall to include additional...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 1, 2018· R & D Systems, Inc.

Recalled Item: Quantikine¿ IVD¿ ELISA Recalled by R & D Systems, Inc. Due to The Human sTfR...

The Issue: The Human sTfR Quantikine IVD ELISA Kit, catalog # DTFR1, lot P180151 was...

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

Class III — Low RiskOngoing
Medical DeviceNovember 1, 2018· ORTHO-CLINICAL DIAGNOSTICS

Recalled Item: VITROS HBeAg Reagent Recalled by ORTHO-CLINICAL DIAGNOSTICS Due to The firm...

The Issue: The firm is extending their previous July 2018 recall to include additional...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 1, 2018· Boston Scientific Corporation

Recalled Item: The SQ-RX Pulse Generator a component of the Subcutaneous Implantable...

The Issue: Experienced accelerated battery depletion and a shortened replacement...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 31, 2018· Cardinal Health 200, LLC

Recalled Item: Protexis Neoprene Surgical Glove Recalled by Cardinal Health 200, LLC Due to...

The Issue: Labeling issue in that the breakthrough (i.e., permeation) times for two...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 31, 2018· Cardinal Health 200, LLC

Recalled Item: Protexis Neoprene Surgical Glove Recalled by Cardinal Health 200, LLC Due to...

The Issue: Labeling issue in that the breakthrough (i.e., permeation) times for two...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 31, 2018· Cardinal Health 200, LLC

Recalled Item: Protexis Neoprene Surgical Glove Recalled by Cardinal Health 200, LLC Due to...

The Issue: Labeling issue in that the breakthrough (i.e., permeation) times for two...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 31, 2018· Foundation Medicine, Inc.

Recalled Item: FoundationOne CDx Test Results Recalled by Foundation Medicine, Inc. Due to...

The Issue: An incorrect test result for a single analyte may have been reported for up...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 31, 2018· Cardinal Health 200, LLC

Recalled Item: Protexis Neoprene Surgical Glove Recalled by Cardinal Health 200, LLC Due to...

The Issue: Labeling issue in that the breakthrough (i.e., permeation) times for two...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 31, 2018· Zimmer Biomet, Inc.

Recalled Item: NexGen¿ Complete Knee Solution Femoral Augment Block Distal only Recalled by...

The Issue: Screw is missing from the package

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 31, 2018· Cardinal Health 200, LLC

Recalled Item: Protexis Neoprene Surgical Glove Recalled by Cardinal Health 200, LLC Due to...

The Issue: Labeling issue in that the breakthrough (i.e., permeation) times for two...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 31, 2018· Cardinal Health 200, LLC

Recalled Item: Protexis Neoprene Surgical Glove Recalled by Cardinal Health 200, LLC Due to...

The Issue: Labeling issue in that the breakthrough (i.e., permeation) times for two...

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

Class II — Potential Health HazardOngoing