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 5032150340 of 54,363 recalls

DrugMay 15, 2013· Novartis Consumer Health

Recalled Item: Excedrin Recalled by Novartis Consumer Health Due to Failed...

The Issue: Failed Impurities/Degradation:Specifications:Unknown degradant found during...

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

Class III — Low RiskOngoing
Refund
DrugMay 15, 2013· Novartis Consumer Health

Recalled Item: Maximum Strength Comtrex Nighttime Cold & Cough Recalled by Novartis...

The Issue: Failed Impurities/Degradation:Specifications:Unknown degradant found during...

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

Class III — Low RiskOngoing
Refund
DrugMay 15, 2013· Novartis Consumer Health

Recalled Item: Maximum Strength Comtrex Recalled by Novartis Consumer Health Due to Failed...

The Issue: Failed Impurities/Degradation:Specifications:Unknown degradant found during...

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

Class III — Low RiskOngoing
Refund
DrugMay 15, 2013· Novartis Consumer Health

Recalled Item: Maximum Strength Comtrex Recalled by Novartis Consumer Health Due to Failed...

The Issue: Failed Impurities/Degradation:Specifications:Unknown degradant found during...

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

Class III — Low RiskOngoing
Refund
Medical DeviceMay 15, 2013· Cincinnati Sub-Zero Products Inc

Recalled Item: Blanketrol III Data Export Software Version 1.10 The Blanketrol III Recalled...

The Issue: During a customer inquiry regarding a beta version of the Bill Data Export...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 14, 2013· Siemens Healthcare Diagnostics, Inc

Recalled Item: ADVIA Centaur¿ iPTH Calibrator 6 pk Recalled by Siemens Healthcare...

The Issue: iPTH Assay- reagent and calibrator lots may have demonstrated higher than...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 14, 2013· GE Healthcare, LLC

Recalled Item: Canister: CO2 canister with GE part numbers 1407-3200-000 Recalled by GE...

The Issue: GE Healthcare has recently become aware of a potential safety issue...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 14, 2013· Siemens Healthcare Diagnostics, Inc

Recalled Item: ADVIA Centaur¿ iPTH ReadyPack Assay 100 Tests Recalled by Siemens Healthcare...

The Issue: iPTH Assay- reagent and calibrator lots may have demonstrated higher than...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 14, 2013· Siemens Healthcare Diagnostics, Inc

Recalled Item: ADVIA Centaur¿ iPTH ReadyPack Assay 500 Tests Recalled by Siemens Healthcare...

The Issue: iPTH Assay- reagent and calibrator lots may have demonstrated higher than...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 14, 2013· Siemens Healthcare Diagnostics, Inc

Recalled Item: ADVIA Centaur iPTH Calibrator 2 pk Recalled by Siemens Healthcare...

The Issue: iPTH Assay- reagent and calibrator lots may have demonstrated higher than...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 14, 2013· Edwards Lifesciences, LLC

Recalled Item: QuickDraw Venous Cannula with Insertion Kit. ThruPort Systmes. Models QD22...

The Issue: Edwards is recalling the QuickDraw Venous Cannula due to complaints of...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 14, 2013· Optovue, Inc.

Recalled Item: Optovue iVue with Normative Database (NDB) with Software Version 3.0...

The Issue: Colors from the NDB comparison for Ganglion Cell Complex thickness in the...

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

Class III — Low RiskOngoing
Medical DeviceMay 13, 2013· Endologix Inc

Recalled Item: Brand Name: AFX" Introducer System Recalled by Endologix Inc Due to...

The Issue: Endologix, Inc. initiated this voluntary recall of certain lots of...

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 13, 2013· Life Technologies Corporation

Recalled Item: HSV 2 Primers Recalled by Life Technologies Corporation Due to Firm received...

The Issue: Firm received complaints that HSV-2 primers failed to amplify HSV-2 DNA.

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 13, 2013· Siemens Medical Solutions USA, Inc

Recalled Item: Siemens AXIOM Artis zeego x-ray Recalled by Siemens Medical Solutions USA,...

The Issue: Siemens issued a customer safety notice about the overlay of system...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 13, 2013· Microgenics Corporation

Recalled Item: Thermo Scientific MAS Bilirubin for Siemens and Dimension Vista Systems...

The Issue: It has been confirmed from in-house testing that Direct Bilirubin (DBIL),...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 13, 2013· Ethicon Endo-Surgery Inc

Recalled Item: ECHELON 60mm Endoscopic Linear Cutter Reloads Black in Flexible Blister...

The Issue: Ethicon Endo-Surgery is initiating a voluntary worldwide recall for ECHELON...

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

Class II — Potential Health HazardOngoing
DrugMay 13, 2013· Zydus Pharmaceuticals USA Inc

Recalled Item: Warfarin Sodium Tablets Recalled by Zydus Pharmaceuticals USA Inc Due to...

The Issue: Failed Tablet/Capsule Specifications: A product complaint was received from...

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

Class I — Serious Health HazardOngoing
Refund
DrugMay 13, 2013· Abrams Royal Pharmacy

Recalled Item: Trace Mineral-5 MDV Recalled by Abrams Royal Pharmacy Due to Non-Sterility;...

The Issue: Non-Sterility; contract laboratory identified Staphylococcus warneri in the...

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

Class I — Serious Health HazardOngoing
Refund
DrugMay 13, 2013· West-ward Pharmaceutical Corp.

Recalled Item: Nicardipine Hydrochloride Injection 25 mg/10 mL (2.5 mg/mL) Recalled by...

The Issue: Failed Impurity/Degradation Specifications; out of specification value for...

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

Class III — Low RiskOngoing
Refund