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. 1,755 recalls have been distributed to North Carolina in the last 12 months.

54,363 total recalls
1,755 in last 12 months

Showing 4502145040 of 54,363 recalls

Medical DeviceAugust 13, 2014· Siemens Medical Solutions USA, Inc.

Recalled Item: V5Ms Transesophageal transducers Recalled by Siemens Medical Solutions USA,...

The Issue: Reports of deterioration of material covering the articulating section of...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 13, 2014· Vapotherm, Inc.

Recalled Item: Vapotherm Precision Flow Recalled by Vapotherm, Inc. Due to Disposable...

The Issue: Disposable Patient Circuit that allows water to leak into the center gas lumen

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 13, 2014· Vapotherm, Inc.

Recalled Item: Vapotherm Precision Flow Recalled by Vapotherm, Inc. Due to Disposable...

The Issue: Disposable Patient Circuit that allows water to leak into the center gas lumen

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 13, 2014· Vapotherm, Inc.

Recalled Item: Vapotherm Precision Flow Recalled by Vapotherm, Inc. Due to Disposable...

The Issue: Disposable Patient Circuit that allows water to leak into the center gas lumen

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 13, 2014· Vapotherm, Inc.

Recalled Item: Vapotherm Precision Flow Recalled by Vapotherm, Inc. Due to Disposable...

The Issue: Disposable Patient Circuit that allows water to leak into the center gas lumen

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 13, 2014· Vapotherm, Inc.

Recalled Item: Vapotherm Precision Flow Recalled by Vapotherm, Inc. Due to Water may leak...

The Issue: Water may leak into the center gas lumen of the Patient Circuit

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 13, 2014· Smith & Nephew, Inc.

Recalled Item: RENASYS EZ Negative Pressure Wound Therapy (NPWT) System (RENASYS EZ)...

The Issue: Modification were made to the RENASYS EZ NPWT Systems without a 510(k) or...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 13, 2014· Vapotherm, Inc.

Recalled Item: Vapotherm Precision Flow Recalled by Vapotherm, Inc. Due to Disposable...

The Issue: Disposable Patient Circuit that allows water to leak into the center gas lumen

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 13, 2014· Vapotherm, Inc.

Recalled Item: Vapotherm Precision Flow Recalled by Vapotherm, Inc. Due to Disposable...

The Issue: Disposable Patient Circuit that allows water to leak into the center gas lumen

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 13, 2014· Maquet Cardiovascular, LLC

Recalled Item: Acrobat V Vacuum Off-Pump System OM-9100S Acrobat SUV Vacuum Off-Pump...

The Issue: An internal finding identified the presence of pinholes/cuts in some of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 13, 2014· Siemens Healthcare Diagnostics

Recalled Item: ADVIA Centaur XP Immunoassay System Recalled by Siemens Healthcare...

The Issue: The firm is conducting a field correction for the ADVIA Centaur and ADVIA...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 13, 2014· Volcano Corporation

Recalled Item: Volcano TrakBack II Disposable Pullback Device Recalled by Volcano...

The Issue: Internal testing had identified a potential breach to the sterile barrier...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 13, 2014· Siemens Healthcare Diagnostics

Recalled Item: ADVIA Centaur Immunoassay System Recalled by Siemens Healthcare Diagnostics...

The Issue: The firm is conducting a field correction for the ADVIA Centaur and ADVIA...

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

Class II — Potential Health HazardOngoing
FoodAugust 13, 2014· McCormick & Company, Inc.

Recalled Item: McCormick Ground Oregano in 0.75 oz plastic bottle. NUMBER: Recalled by...

The Issue: Retail sample of ground oregano tested positive for Salmonella.

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

Class I — Serious Health HazardOngoing
Refund
DrugAugust 13, 2014· VistaPharm, Inc.

Recalled Item: METOCLOPRAMIDE ORAL SOLUTION Recalled by VistaPharm, Inc. Due to Defective...

The Issue: Defective Container: Product leaks when inverted.

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 13, 2014· Fresenius Kabi USA, LLC

Recalled Item: PROPRANOLOL HYDROCHLORIDE INJECTION Recalled by Fresenius Kabi USA, LLC Due...

The Issue: CGMP Deviations: Citations given to API supplier by the Italian Health...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceAugust 12, 2014· Siemens Medical Solutions USA, Inc

Recalled Item: AXIOM Luminos dRF system with SW VD10 or on Luminos Recalled by Siemens...

The Issue: It was determined that a potential malfunction may occur on the Luminos dRF...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 12, 2014· Gendex Corp

Recalled Item: eXpertDC intraoral x-ray Recalled by Gendex Corp Due to Two (2) failures of...

The Issue: Two (2) failures of the spring link components within the articulated arm...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 12, 2014· Ethicon Endo-Surgery Inc

Recalled Item: PROXIMATE Skin Stapler. PROXIMATE RH Rotating-Head Skin Stapler (Model...

The Issue: The device may have a non-conforming component that may cause the device to...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 11, 2014· Primus Medical LLC

Recalled Item: Prime Care ¿ Transcend Mattress Recalled by Primus Medical LLC Due to The...

The Issue: The firm found that the top cover of the mattresses were delaminating.

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

Class II — Potential Health HazardOngoing