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. 1,862 recalls have been distributed to North Carolina in the last 12 months.

54,363 total recalls
1,862 in last 12 months

Showing 3276132780 of 54,363 recalls

FoodMarch 22, 2017· Whiskey Hill Smokehouse

Recalled Item: Elk Jerky Recalled by Whiskey Hill Smokehouse Due to Undeclared Soy

The Issue: Elk jerky is recalled due to undeclared soy lecithin.

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

Class II — Potential Health HazardOngoing
Refund
FoodMarch 22, 2017· Whiskey Hill Smokehouse

Recalled Item: Bison Jerky Recalled by Whiskey Hill Smokehouse Due to Undeclared Soy

The Issue: Bison jerky is recalled due to undeclared soy lecithin.

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

Class II — Potential Health HazardOngoing
Refund
FoodMarch 22, 2017· Whiskey Hill Smokehouse

Recalled Item: Kangaroo jerky Recalled by Whiskey Hill Smokehouse Due to Undeclared Soy

The Issue: kangaroo jerky is recalled due to undeclared soy lecithin.

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMarch 22, 2017· Tosoh Bioscience Inc

Recalled Item: AIA-360 Analyzer is capable of performing two methods of immunoassay:...

The Issue: The firm has become aware of a potential issue with the AIA-360 analyzer...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 22, 2017· Cook Medical Incorporated

Recalled Item: Zenith Alpha Thoracic Endovascular Graft The Zenith Alpha" Thoracic...

The Issue: There have been five reports of graft thrombosis/occlusion during global...

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 22, 2017· ReFlow Medical

Recalled Item: Wingman 35 Crossing Catheter Recalled by Medical Due to Medical is recalling...

The Issue: Medical is recalling the Wingman 35 Crossing Catheter because it may be...

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 22, 2017· Zimmer Biomet, Inc.

Recalled Item: Regenerex Patella RGX 3 PEG SER A PATELLA 28MM RGX Recalled by Zimmer...

The Issue: pegs shearing post-operatively

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 22, 2017· Philips Electronics North America Corporation

Recalled Item: Allura Xper Release 8.2 (Laird chiller is always installed) Recalled by...

The Issue: Due to a leak in the detector cooling system, cooling liquid may leak...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 22, 2017· Philips Electronics North America Corporation

Recalled Item: The following systems are only affected if a Laird chiller Recalled by...

The Issue: Due to a leak in the detector cooling system, cooling liquid may leak...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 22, 2017· Philips Electronics North America Corporation

Recalled Item: UNIQ: UNIQ FD10 722026 Recalled by Philips Electronics North America...

The Issue: Due to a leak in the detector cooling system, cooling liquid may leak...

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

Class II — Potential Health HazardOngoing
DrugMarch 21, 2017· Mylan Institutional, Inc. (d.b.a. UDL Laboratories)

Recalled Item: Atorvastatin Calcium Tablets Recalled by Mylan Institutional, Inc. (d.b.a....

The Issue: Microbial Contamination of Non-Sterile Products: potential of an elevated...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMarch 21, 2017· Roche Diagnostics Corporation

Recalled Item: Sample probes associated with: cobas 6000 Series System Recalled by Roche...

The Issue: Due to a design change in 2015, corrosion on the sample probe electrical...

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

Class II — Potential Health HazardOngoing
DrugMarch 20, 2017· Valeant Pharmaceuticals North America LLC

Recalled Item: CLENZIderm M.D. Pore Therapy Salicylic Acid 2% Acne Treatment 5 fl. oz. (148...

The Issue: Discoloration.

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

Class III — Low RiskOngoing
Refund
DrugMarch 20, 2017· Valeant Pharmaceuticals North America LLC

Recalled Item: CLENZIderm M.D. Acne Treatment System Recalled by Valeant Pharmaceuticals...

The Issue: Discoloration.

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

Class III — Low RiskOngoing
Refund
DrugMarch 20, 2017· G & W Laboratories, Inc.

Recalled Item: Ciclopirox Olamine Cream USP Recalled by G & W Laboratories, Inc. Due to...

The Issue: Labeling: Incorrect or Missing Package Insert: product lots packaged with an...

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

Class III — Low RiskOngoing
Refund
DrugMarch 20, 2017· Mylan Pharmaceuticals Inc.

Recalled Item: Atorvastatin Calcium Tablets Recalled by Mylan Pharmaceuticals Inc. Due to...

The Issue: Microbial Contamination of Non-Sterile Products: potential of an elevated...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 20, 2017· Mylan Pharmaceuticals Inc.

Recalled Item: Atorvastatin Calcium Tablets Recalled by Mylan Pharmaceuticals Inc. Due to...

The Issue: Microbial Contamination of Non-Sterile Products: potential of an elevated...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 20, 2017· Mylan Pharmaceuticals Inc.

Recalled Item: Atorvastatin Calcium Tablets Recalled by Mylan Pharmaceuticals Inc. Due to...

The Issue: Microbial Contamination of Non-Sterile Products: potential of an elevated...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 20, 2017· Mylan Pharmaceuticals Inc.

Recalled Item: Atorvastatin Calcium Tablets Recalled by Mylan Pharmaceuticals Inc. Due to...

The Issue: Microbial Contamination of Non-Sterile Products: potential of an elevated...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMarch 20, 2017· Arrow International Inc

Recalled Item: AGB+ Pressure Injectable Multi-Lumen CVC Kit intended to permit venous...

The Issue: Arrow International initiated the recall due to reports of safety cover...

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

Class II — Potential Health HazardOngoing