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. 857 recalls have been distributed to North Carolina in the last 12 months.

54,363 total recalls
857 in last 12 months

Showing 52821–52840 of 54,363 recalls

FoodJuly 26, 2012· Ken's Foods, Inc.

Recalled Item: Tartar Sauce sold under the following brand names: 1) Golden Corral Tartar...

The Issue: Products manufactured with Gills Onions recalled due to potential for...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceJuly 26, 2012· St. Jude Medical

Recalled Item: Eon Mini - 3788 (IPG) Recalled by St. Jude Medical Due to As part of St....

The Issue: As part of St. Jude Medical's routine tracking and product monitoring, they...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 26, 2012· St. Jude Medical

Recalled Item: Eon - 3701 (Wall Charger) and 3711 (Portable Charger). Product Recalled by...

The Issue: St. Jude Medical has informed your doctor that a number of cases have been...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 26, 2012· St. Jude Medical

Recalled Item: Eon Mini - 3721 (Charger). Product Usage: Eon Mini system Recalled by St....

The Issue: St. Jude Medical has informed your doctor that a number of cases have been...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 26, 2012· Philips Medical Systems North America Co. Phillips

Recalled Item: Philips HeartStart FRx 861304 Automated External Defibrillator Manufactured...

The Issue: Philips determined that it is important to clarify information in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 26, 2012· Philips Medical Systems North America Co. Phillips

Recalled Item: Philips and Laerdal brands of HeartStart HS1 Defibrillator Family Model...

The Issue: Philips determined that it is important to clarify information in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 26, 2012· Stryker Orthobiologics, Inc.

Recalled Item: Styker Orthobiologics Vita Plasma Separator Recalled by Stryker...

The Issue: When preparing plasma using VitaPrep, it was reported that a small amount of...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 26, 2012· Terumo Cardiovascular Systems Corporation

Recalled Item: Serial interface module RS-232 Product Usage: The System 1 provides Recalled...

The Issue: Terumo Cardiovascular Systems has received reports of malfunctions involving...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 26, 2012· Terumo Cardiovascular Systems Corporation

Recalled Item: Interface module for CDl System 500 Product Usage: The Interface Recalled by...

The Issue: Terumo Cardiovascular Systems has received reports of malfunctions involving...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 26, 2012· Terumo Cardiovascular Systems Corporation

Recalled Item: Interface module for CDl System 100/101 Product Usage: The Interface...

The Issue: Terumo Cardiovascular Systems has received reports of malfunctions involving...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 26, 2012· Terumo Cardiovascular Systems Corporation

Recalled Item: Serial interface module RS-485 Product Usage: The System 1 provides Recalled...

The Issue: Terumo Cardiovascular Systems has received reports of malfunctions involving...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 26, 2012· Terumo Cardiovascular Systems Corporation

Recalled Item: System 1 base 220/240V The Terumo Advanced Perfusion System 1 Recalled by...

The Issue: Terumo Cardiovascular Systems sent a Safety Advisory (AA-2010-007-C) on...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 26, 2012· Terumo Cardiovascular Systems Corporation

Recalled Item: System 1 base 100/120V The Terumo Advanced Perfusion System 1 Recalled by...

The Issue: Terumo Cardiovascular Systems sent a Safety Advisory (AA-2010-007-C) on...

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

Class II — Potential Health HazardOngoing
DrugJuly 25, 2012· Lloyd Inc. of Iowa

Recalled Item: Levothroid (levothyroxine sodium tablets Recalled by Lloyd Inc. of Iowa Due...

The Issue: Subpotent; 9-month stability interval

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 25, 2012· Lloyd Inc. of Iowa

Recalled Item: Levothroid (levothyroxine sodium tablets Recalled by Lloyd Inc. of Iowa Due...

The Issue: Subpotent; 9-month stability interval

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 25, 2012· Lloyd Inc. of Iowa

Recalled Item: Thyro-Tab 0.075 mg. Recalled by Lloyd Inc. of Iowa Due to Subpotent; 9-month...

The Issue: Subpotent; 9-month stability interval

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 25, 2012· Lloyd Inc. of Iowa

Recalled Item: Thyro-Tab 0.050 mg. Recalled by Lloyd Inc. of Iowa Due to Subpotent; 9-month...

The Issue: Subpotent; 9-month stability interval

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 25, 2012· American Health Packaging

Recalled Item: Topiramate Tablets Recalled by American Health Packaging Due to Labeling:...

The Issue: Labeling: Label Mix-Up: A typographical error in the product form on the...

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

Class III — Low RiskOngoing
Refund
FoodJuly 25, 2012· Freshpoint Atlanta, Inc.

Recalled Item: Processed Yellow Onions - Veg. Mirepoix Recalled by Freshpoint Atlanta, Inc....

The Issue: Product may be contaminated with Listeria monocytogenes.

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

Class I — Serious Health HazardOngoing
Refund
FoodJuly 25, 2012· Freshpoint Atlanta, Inc.

Recalled Item: Processed Yellow Onions - Whole Peeled Recalled by Freshpoint Atlanta, Inc....

The Issue: Product may be contaminated with Listeria monocytogenes.

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

Class I — Serious Health HazardOngoing
Refund