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 4498145000 of 54,363 recalls

Medical DeviceAugust 21, 2014· Beckman Coulter Inc.

Recalled Item: UniCel 600/800 Access Immunoassay Systems are in vitro diagnostic devices...

The Issue: Beckman Coulter is recalling the Sample Probe Cable because nonconforming...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 21, 2014· Philips Medical Systems, Inc.

Recalled Item: Ingenia Recalled by Philips Medical Systems, Inc. Due to When a fused series...

The Issue: When a fused series of a sagittal, coronal or radial multi station scan is...

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

Class II — Potential Health HazardOngoing
FoodAugust 21, 2014· Nestle USA, Inc.

Recalled Item: Lean Cuisine Culinary Collection Chicken with Peanut Sauce. Packaged in...

The Issue: Nestl¿ Prepared Foods Company Announces Allergy Alert and Voluntary Recall...

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

Class I — Serious Health HazardOngoing
Refund
DrugAugust 21, 2014· Apotex Corp.

Recalled Item: Candesartan Cilexetil and Hydrochlorothiazide Tablets 32 mg/12.5 mg Recalled...

The Issue: Failed Impurity/Degradation Specification; high out of specification for CAD...

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

Class III — Low RiskOngoing
Refund
DrugAugust 20, 2014· ChiroNutraceutical LLC

Recalled Item: CHIROTHIN Dietary Supplement Recalled by ChiroNutraceutical LLC Due to...

The Issue: Marketed without an Approved NDA/ANDA; Product contains unapproved hHCG.

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

Class III — Low RiskOngoing
Refund
Medical DeviceAugust 20, 2014· Ortho-Clinical Diagnostics

Recalled Item: VITROS Chemistry Products PHYT (Phenytoin) Slides Recalled by Ortho-Clinical...

The Issue: Ortho Clinical Diagnostics identified a potential for biased results to be...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 19, 2014· Philips Medical Systems, Inc.

Recalled Item: Patient Support Material Number: 9890 010 87431 used with: BuckyDiagnost...

The Issue: The hook does not securely hold the footplate in vertical position....

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 19, 2014· ICU Medical, Inc.

Recalled Item: 98" (249 cm) Appx 12.3 ml Recalled by ICU Medical, Inc. Due to ICU is...

The Issue: ICU is recalling the ConMed Stat 2 flow controller because it may deliver a...

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

Class I — Serious Health HazardOngoing
Medical DeviceAugust 19, 2014· St Jude Medical Cardiac Rhythm Management Division

Recalled Item: Ellipse Implantable Cardioverter Defibrillators (ICDs) Recalled by St Jude...

The Issue: An anomaly may result in delayed, partial, or no delivery of high voltage...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 19, 2014· ICU Medical, Inc.

Recalled Item: STAT 2 Flow Controller Recalled by ICU Medical, Inc. Due to ICU is recalling...

The Issue: ICU is recalling the ConMed Stat 2 flow controller because it may deliver a...

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

Class I — Serious Health HazardOngoing
Medical DeviceAugust 19, 2014· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Siemens CentraLink Data Management System Recalled by Siemens Healthcare...

The Issue: Siemens Healthcare Diagnostics has identified a task scheduler issue with...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 19, 2014· ICU Medical, Inc.

Recalled Item: 83" (211 cm) Appx 10.3 mL Recalled by ICU Medical, Inc. Due to ICU is...

The Issue: ICU is recalling the ConMed Stat 2 flow controller because it may deliver a...

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

Class I — Serious Health HazardOngoing
Medical DeviceAugust 19, 2014· Philips Medical Systems, Inc.

Recalled Item: Patient Support Material Number: 9890 010 87431 Recalled by Philips Medical...

The Issue: The hook does not securely hold the footplate in vertical position....

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 19, 2014· ICU Medical, Inc.

Recalled Item: STAT 2 Flow Controller Recalled by ICU Medical, Inc. Due to ICU is recalling...

The Issue: ICU is recalling the ConMed Stat 2 flow controller because it may deliver a...

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

Class I — Serious Health HazardOngoing
Medical DeviceAugust 18, 2014· Elekta, Inc.

Recalled Item: FOCAL Sim Workstation Recalled by Elekta, Inc. Due to When DICOM is...

The Issue: When DICOM is exporting an arc plan (VMAT, Dynamic Conformal of 3D Static...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 18, 2014· Varian Medical Systems, Inc.

Recalled Item: 4D Integrated Treatment Console (4DITC) Recalled by Varian Medical Systems,...

The Issue: Due to user error, the 4DITC can improperly allow users to clear a safety...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 18, 2014· Integra LifeSciences Corp.

Recalled Item: Integra Licox Pt02 Monitor Recalled by Integra LifeSciences Corp. Due to...

The Issue: Integra LifeSciences Corporation received 2 complaints that the USB port on...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 18, 2014· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Siemens Dimension Vista¿ CHEM 1 CAL Recalled by Siemens Healthcare...

The Issue: Siemens Healthcare Diagnostics has received complaints for low recovery of...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 18, 2014· Hitachi Medical Systems America Inc

Recalled Item: Hitachi Echelon Oval MRI system is a diagnostic imaging device Recalled by...

The Issue: The Gradient Coil was found to have a failure mode that allowed it to...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 18, 2014· Elekta, Inc.

Recalled Item: Monaco The Monaco system is used to make treatment plans Recalled by Elekta,...

The Issue: Incorrect Delivery of Composite VMAT Fields - When DICOM is exporting an arc...

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

Class II — Potential Health HazardOngoing