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. 1,932 recalls have been distributed to North Carolina in the last 12 months.

54,363 total recalls
1,932 in last 12 months

Showing 2034120360 of 29,737 recalls

Medical DeviceSeptember 14, 2016· Hand Biomechanics Lab Inc

Recalled Item: Agee-WristJack¿ Fracture Reduction System Recalled by Hand Biomechanics Lab...

The Issue: A number of Agee WristJack¿ Fracture Reduction Systems have been...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 13, 2016· TEM Systems Inc

Recalled Item: ex-TEM Assay for ROTEM delta Thromboelastometry System. Art. no.: 503-05 US...

The Issue: Customers complained of low/empty reagent vials.

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 13, 2016· Tearscience, Inc

Recalled Item: LipiFlow thermal Pulsation System Recalled by Tearscience, Inc Due to...

The Issue: Complaints related to an error condition occurring during patient treatment...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 9, 2016· Teleflex Medical

Recalled Item: Teleflex Percuaneous Solutions Recalled by Teleflex Medical Due to The...

The Issue: The product is being recalled due to a labeling error. The Gripper Graspers...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 9, 2016· Contour Fabricators Inc

Recalled Item: Zero-Gravity Radiation Protection System Radiology Personnel protective...

The Issue: Two customer complaints suggest that excessive rotation of the cable in one...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 9, 2016· Teleflex Medical

Recalled Item: Teleflex Percuaneous Solutions Recalled by Teleflex Medical Due to The...

The Issue: The product is being recalled due to a labeling error. The Gripper Graspers...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 7, 2016· Angiodynamics Inc. (Navilyst Medical Inc.)

Recalled Item: Celerity ECG Cable Accessory Pack Recalled by Angiodynamics Inc. (Navilyst...

The Issue: The Celerity ECG Cable Accessory Pack has the potential to contain an ECG...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 7, 2016· Ortho-Clinical Diagnostics

Recalled Item: enGen Laboratory Automation System (Product Code ENGEN) configured with...

The Issue: Ortho confirmed that it is possible for the mis-association of sample...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 6, 2016· Siemens Medical Solutions USA, Inc

Recalled Item: Syngo.plaza VB10A Recalled by Siemens Medical Solutions USA, Inc Due to...

The Issue: Software upgrade to eliminate several issues

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 6, 2016· Siemens Medical Solutions USA, Inc

Recalled Item: Syngo.plaza Recalled by Siemens Medical Solutions USA, Inc Due to Software...

The Issue: Software upgrade to eliminate several issues

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 2, 2016· Arrow International Inc

Recalled Item: HANDS-OFF Infusion Port Thermodilution Catheter consists of the Arrow IPTD...

The Issue: Labeling inconsistency

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 2, 2016· Siemens Healthcare Diagnostics Inc

Recalled Item: Siemens RAPIDPoint 400 Measurement Cartridge Siemens SMN numbers:10329756...

The Issue: Error in the value assignment for the Chloride calibrators in the RAPIDPoint...

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

Class III — Low RiskOngoing
Medical DeviceSeptember 2, 2016· Siemens Healthcare Diagnostics Inc

Recalled Item: Siemens RAPIDPoint 405 Measurement Cartridge Siemens SMN numbers: 10844812...

The Issue: Error in the value assignment for the Chloride calibrators in the RAPIDPoint...

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

Class III — Low RiskOngoing
Medical DeviceSeptember 2, 2016· Heritage Medical Products, Inc.

Recalled Item: 2000 Vascular with 30 Degree option Recalled by Heritage Medical Products,...

The Issue: Potential for bed to drop suddenly at the head while a patient is laying on it.

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 1, 2016· RAYSEARCH LABORATORIES AB

Recalled Item: RayStation 2.5 Recalled by RAYSEARCH LABORATORIES AB Due to RaySearch became...

The Issue: RaySearch became aware of the problem as it was discovered in cooperation...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 31, 2016· Ormco/Sybronendo

Recalled Item: Sealapex Xpress Recalled by Ormco/Sybronendo Due to SybronEndo is recalling...

The Issue: SybronEndo is recalling the Sealapex Xpress because it was labeled with an...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 31, 2016· GE Healthcare, LLC

Recalled Item: GE Healthcare SIGNA Creator Recalled by GE Healthcare, LLC Due to GE...

The Issue: GE Healthcare is conducting a recall dealing with an incorrect RF Power...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 30, 2016· Siemens Healthcare Diagnostics, Inc.

Recalled Item: IMMULITE 2000/IMMULITE 2000XPi Systems CMM CMV IgM Assay Recalled by Siemens...

The Issue: Multiple customers reported seeing an increase in imprecision with some...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 30, 2016· Siemens Healthcare Diagnostics, Inc.

Recalled Item: IMMULITE/ IMMULITE 1000 Systems CMM CMV IgM Assay Recalled by Siemens...

The Issue: Multiple customers reported seeing an increase in imprecision with some...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 30, 2016· ErgoSafe Products, LLC (DBA) Prism Medical

Recalled Item: Carry bar which is an accessory to a lift used Recalled by ErgoSafe...

The Issue: The black plastic puck on the carry bar is breaking resulting in potential...

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

Class II — Potential Health HazardOngoing