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. 1,744 recalls have been distributed to North Carolina in the last 12 months.

54,363 total recalls
1,744 in last 12 months

Showing 4818148200 of 54,363 recalls

DrugOctober 21, 2013· Medisca Inc.

Recalled Item: Human Chorionic Gonadotropin Recalled by Medisca Inc. Due to Labeling: Label...

The Issue: Labeling: Label Error on Declared Strength; Firm states that erroneous...

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

Class I — Serious Health HazardOngoing
Refund
FoodOctober 21, 2013· Apex Energetics

Recalled Item: LGS-Zyme (Z12) Recalled by Apex Energetics Due to Apex Energetics is...

The Issue: Apex Energetics is recalling GlutenFlam, SuperDigestZyme, LGS-Zyme, and...

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

Class II — Potential Health HazardOngoing
Refund
FoodOctober 21, 2013· Apex Energetics

Recalled Item: SuperDigestZyme (Z22) Recalled by Apex Energetics Due to Apex Energetics is...

The Issue: Apex Energetics is recalling GlutenFlam, SuperDigestZyme, LGS-Zyme, and...

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

Class II — Potential Health HazardOngoing
Refund
FoodOctober 21, 2013· Apex Energetics

Recalled Item: GlutenFlam (K-52) Enzyme & Bioflavonoid Dietary Supplement Recalled by Apex...

The Issue: Apex Energetics is recalling GlutenFlam, SuperDigestZyme, LGS-Zyme, and...

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

Class II — Potential Health HazardOngoing
Refund
FoodOctober 21, 2013· Apex Energetics

Recalled Item: RepairVite (K63) Recalled by Apex Energetics Due to Apex Energetics is...

The Issue: Apex Energetics is recalling GlutenFlam, SuperDigestZyme, LGS-Zyme, and...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceOctober 21, 2013· Medtronic Vascular

Recalled Item: ATTAIN HYBRID¿ Guide Wire Recalled by Medtronic Vascular Due to Potential...

The Issue: Potential for PTFE (polytetrafluroethylene) coating to delaminate and detach...

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

Class I — Serious Health HazardOngoing
Medical DeviceOctober 21, 2013· Applied Medical Resources Corp

Recalled Item: Applied Medical's Inzii¿ 12/15mm Retrieval System. Applieds Inzii Tissue...

The Issue: Applied Medical is conducting a voluntary recall of the Inzii¿ 12/15mm...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 21, 2013· Urologix, Inc.

Recalled Item: Prostiva RF Therapy Hand Piece Kit Recalled by Urologix, Inc. Due to A Hand...

The Issue: A Hand Piece high deployment force exceeded the maximum specification.

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 21, 2013· Medtronic Vascular

Recalled Item: Cougar¿ Nitinol Workhorse Guidewire: Models: CGRLS190HJ Recalled by...

The Issue: Potential for PTFE (polytetrafluroethylene) coating to delaminate and detach...

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

Class I — Serious Health HazardOngoing
Medical DeviceOctober 21, 2013· Medtronic Vascular

Recalled Item: Zinger¿ Stainless Steel Workhorse Guidewire Recalled by Medtronic Vascular...

The Issue: Potential for PTFE (polytetrafluroethylene) coating to delaminate and detach...

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

Class I — Serious Health HazardOngoing
Medical DeviceOctober 21, 2013· Medtronic Vascular

Recalled Item: THUNDER¿ Extra Support Guidewire Recalled by Medtronic Vascular Due to...

The Issue: Potential for PTFE (polytetrafluroethylene) coating to delaminate and detach...

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

Class I — Serious Health HazardOngoing
Medical DeviceOctober 21, 2013· Medtronic Vascular

Recalled Item: THUNDER¿ Steerable Guidewire Recalled by Medtronic Vascular Due to Potential...

The Issue: Potential for PTFE (polytetrafluroethylene) coating to delaminate and detach...

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

Class I — Serious Health HazardOngoing
Medical DeviceOctober 21, 2013· Intuitive Surgical, Inc.

Recalled Item: da Vinci Vision System Cart Recalled by Intuitive Surgical, Inc. Due to...

The Issue: Intuitive has identified that the metalized coating on the IS3000 HD lamp...

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

Class III — Low RiskOngoing
Medical DeviceOctober 21, 2013· Medtronic Vascular

Recalled Item: COUGAR¿ Steerable Guidewire Recalled by Medtronic Vascular Due to Potential...

The Issue: Potential for PTFE (polytetrafluroethylene) coating to delaminate and detach...

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

Class I — Serious Health HazardOngoing
Medical DeviceOctober 21, 2013· Vital Images, Inc.

Recalled Item: VitreaCore¿ software. Versions subject to the limitation: 6.0 Recalled by...

The Issue: Vital Images, Inc. has found an issue in VitreaCore software though internal...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 21, 2013· Medtronic Vascular

Recalled Item: ZINGER¿ Steerable Guidewire Recalled by Medtronic Vascular Due to Potential...

The Issue: Potential for PTFE (polytetrafluroethylene) coating to delaminate and detach...

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

Class I — Serious Health HazardOngoing
Medical DeviceOctober 21, 2013· Medtronic Vascular

Recalled Item: ProVia¿ CROSSING GUIDEWIRE Recalled by Medtronic Vascular Due to Potential...

The Issue: Potential for PTFE (polytetrafluroethylene) coating to delaminate and detach...

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

Class I — Serious Health HazardOngoing
Medical DeviceOctober 18, 2013· Advanced Sterilization Products

Recalled Item: Sterrad 100NX Recalled by Advanced Sterilization Products Due to Advanced...

The Issue: Advanced Sterilization Products (ASP) is recalling the Sterrad 100NX...

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

Class II — Potential Health HazardOngoing
DrugOctober 18, 2013· Compounding Centre At Blue Ridge

Recalled Item: Triple Mix Injectable (aka Dr Ungers Triple Rx Recalled by Compounding...

The Issue: Lack of Assurance of Sterility; All lots of sterile products compounded by...

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 18, 2013· Compounding Centre At Blue Ridge

Recalled Item: Papaverine/Phentolamine 30 mg/mL/2.0 mg/mL Inj Recalled by Compounding...

The Issue: Lack of Assurance of Sterility; All lots of sterile products compounded by...

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

Class II — Potential Health HazardOngoing
Refund