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 3346133480 of 54,363 recalls

FoodJanuary 24, 2017· Circle U Foods, Inc

Recalled Item: Circle U Foods Recalled by Circle U Foods, Inc Due to Potential glass...

The Issue: Potential glass inclusion

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

Class II — Potential Health HazardOngoing
Refund
FoodJanuary 24, 2017· Circle U Foods, Inc

Recalled Item: Circle U Foods Recalled by Circle U Foods, Inc Due to Potential glass inclusion

The Issue: Potential glass inclusion

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

Class II — Potential Health HazardOngoing
Refund
FoodJanuary 24, 2017· Circle U Foods, Inc

Recalled Item: Circle U Foods Recalled by Circle U Foods, Inc Due to Potential glass...

The Issue: Potential glass inclusion

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

Class II — Potential Health HazardOngoing
Refund
FoodJanuary 24, 2017· Circle U Foods, Inc

Recalled Item: Circle U Foods Recalled by Circle U Foods, Inc Due to Potential glass...

The Issue: Potential glass inclusion

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJanuary 23, 2017· Strata Skin Sciences, Inc.

Recalled Item: XTRAC Excimer Laser Recalled by Strata Skin Sciences, Inc. Due to When the...

The Issue: When the Liquid Guide ( LLG) is not used according to the operator manual,...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 23, 2017· Covidien LLC

Recalled Item: Premier Guard Drape Recalled by Covidien LLC Due to Sterility compromised...

The Issue: Sterility compromised due to breach in sterile barrier

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 23, 2017· Covidien LLC

Recalled Item: Premier Guard Sterile Drape For Use with Blair-Port Wand (02-0029) Recalled...

The Issue: Sterility compromised due to breach in sterile barrier

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

Class II — Potential Health HazardOngoing
FoodJanuary 20, 2017· NOW Foods

Recalled Item: NOW¿ Multi-Food 1 Tablets Recalled by NOW Foods Due to Product's supplement...

The Issue: Product's supplement fact panel incorrectly states that the product contains...

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

Class III — Low RiskOngoing
Refund
FoodJanuary 20, 2017· Yum Retaurants International

Recalled Item: Pizza Hut Creamy Alfredo sauce Recalled by Yum Retaurants International Due...

The Issue: Foreign object in alfredo sauce. Likely flexible plastic.

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

Class III — Low RiskOngoing
Refund
Medical DeviceJanuary 20, 2017· Metrex Research, LLC.

Recalled Item: CaviWipes1 Extra Large Recalled by Metrex Research, LLC. Due to Metrex is...

The Issue: Metrex is recalling the CaviWipes Extra Large because they may have been...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 20, 2017· Atrium Medical Corporation

Recalled Item: Atrium PVC 8 Fr Straight Thoracic Catheter Code Number: 8008 Recalled by...

The Issue: Labeling icon depicts a catheter having six (6) eyelets; however the correct...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 20, 2017· Integra LifeSciences Corp.

Recalled Item: Integra Cadence Total Ankle System Recalled by Integra LifeSciences Corp....

The Issue: Posterior tibial fractures have been reported.

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 20, 2017· Atrium Medical Corporation

Recalled Item: Atrium PVC 10 Fr Straight Thoracic Catheter Code Number: 8010 Recalled by...

The Issue: Labeling icon depicts a catheter having six (6) eyelets; however the correct...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 20, 2017· GE Healthcare, LLC

Recalled Item: Discovery MR450 The systems are whole body magnetic resonance scanners...

The Issue: Potential safety issue with the patient bore heating on the Discovery MR450...

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

Class II — Potential Health HazardOngoing
DrugJanuary 19, 2017· Mylan Pharmaceuticals Inc.

Recalled Item: Mirtazapine Tablets Recalled by Mylan Pharmaceuticals Inc. Due to Presence...

The Issue: Presence of Foreign Tablets/Capsules; possibility of Glipizide 10 mg tablet...

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 19, 2017· LEO PHARMA INC

Recalled Item: Calcipotriene Cream 0.0005% Recalled by LEO PHARMA INC Due to Undeclared...

The Issue: Incorrect/Undeclared excipients: inadvertent omission of a drug excipient...

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 19, 2017· Mylan Pharmaceuticals Inc.

Recalled Item: glipiZIDE Extended-Release Tablets Recalled by Mylan Pharmaceuticals Inc....

The Issue: Presence of Foreign Tablets/Capsules; bottles of Glipizide 5 mg tablets may...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJanuary 19, 2017· Applied Medical Technology Inc

Recalled Item: AMT 12 inch Right Angle Feeding Set with Y-Port Used Recalled by Applied...

The Issue: Expired expiration dates are listed on the pouches.

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

Class III — Low RiskOngoing
Medical DeviceJanuary 19, 2017· Applied Medical Technology Inc

Recalled Item: AMT Bridle - Nasal Tube Retaining System Used with...

The Issue: Expired expiration dates are listed on the pouches.

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

Class III — Low RiskOngoing
DrugJanuary 18, 2017· VistaPharm, Inc.

Recalled Item: Potassium Chloride Oral Solution Recalled by VistaPharm, Inc. Due to...

The Issue: Defective Container: Leakage of unit dose cups that may occur at the seal.

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

Class II — Potential Health HazardOngoing
Refund