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. 1,924 recalls have been distributed to North Carolina in the last 12 months.

54,363 total recalls
1,924 in last 12 months

Showing 2094120960 of 29,737 recalls

Medical DeviceMay 10, 2016· Medical Vision Ab

Recalled Item: Double Pump RF Patient Cassette Recalled by Medical Vision Ab Due to...

The Issue: Sterility of device may be compromised due to sterile package breakage.

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 9, 2016· GE Healthcare, LLC

Recalled Item: MSK 1.5T Extreme MR Scanner Recalled by GE Healthcare, LLC Due to The gas...

The Issue: The gas venting may not occur properly. A site reported a magnet quenching...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 9, 2016· Roche Molecular Systems, Inc.

Recalled Item: cobas¿ Liat¿ Analyzer Recalled by Roche Molecular Systems, Inc. Due to...

The Issue: Device was released with default pcal/gain settings for photometers instead...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 9, 2016· ORTHO-CLINICAL DIAGNOSTICS

Recalled Item: VITROS Immunodiagnostic Products AFP Reagent Pack Recalled by ORTHO-CLINICAL...

The Issue: Ortho Clinical Diagnostics (OCD) confirmed that specific lots of VITROS...

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

Class III — Low RiskOngoing
Medical DeviceMay 9, 2016· Immuno-Mycologics, Inc

Recalled Item: Histoplasma Yeast Complement Fixation Antigen Dilute Ref# H30150 The fungal...

The Issue: The device was found to have bacterial contamination.

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 9, 2016· GE Healthcare, LLC

Recalled Item: GE Revolution CT The system is intended for head Recalled by GE Healthcare,...

The Issue: GEHC has become aware of a potential safety issue in the Revolution CT...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 9, 2016· GE Healthcare, LLC

Recalled Item: Optima 1.5T MR430s MR Scanner Recalled by GE Healthcare, LLC Due to The gas...

The Issue: The gas venting may not occur properly. A site reported a magnet quenching...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 6, 2016· Custom Ultrasonics, Inc.

Recalled Item: The System 83 Plus Recalled by Custom Ultrasonics, Inc. Due to To warn...

The Issue: To warn customers that Custom Ultrasonics, Inc. System 83 Plus AERs should...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 6, 2016· Leica Biosystems Richmond Inc.

Recalled Item: Ariol is an automated scanning microscope and image analysis system....

The Issue: An issue during the manufacturing process caused systems to have an...

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

Class III — Low RiskOngoing
Medical DeviceMay 6, 2016· BEST THERATRONICS LTD.

Recalled Item: Best Theratronics cabinet x-ray systems intended for use in the Recalled by...

The Issue: It was discovered that both the new device and the predicate device failed...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 5, 2016· Ellipse A/S

Recalled Item: Ellipse ND: YAG Laser applicator for Ellipse Nordlys system Medical Recalled...

The Issue: Failure to provide the required instructions specifying a procedure and...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 5, 2016· Ellipse A/S

Recalled Item: Ellipse ND: YAG Laser applicator for Ellipse Multiflex Medical Laser...

The Issue: Failure to provide the required instructions specifying a procedure and...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 5, 2016· Medical Components, Inc dba MedComp

Recalled Item: Tearaway Introducer Recalled by Medical Components, Inc dba MedComp Due to...

The Issue: This recall has been initiated due to the product labeled with the incorrect...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 5, 2016· Teleflex Medical

Recalled Item: Sterile Sheridan/HVT Cuffed Recalled by Teleflex Medical Due to The labeling...

The Issue: The labeling of some units indicates that it contains a size 7mm tracheal...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 5, 2016· Stryker Medical Division of Stryker Corporation

Recalled Item: Stryker PowerPRO (XT Recalled by Stryker Medical Division of Stryker...

The Issue: Complaints of smoke coming from the foot end of the cot. This reportedly...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 4, 2016· Zimmer Manufacturing B.V.

Recalled Item: Zimmer universal locking system (ULS) 3.5 mm cortical screw selftapping...

The Issue: A small hole may be present in the inner tray of specific lots of sterile...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 4, 2016· Zimmer Manufacturing B.V.

Recalled Item: Zimmer Plates and Screws (ZPS) 3.5 mm Cortical Screw SelfTapping Recalled by...

The Issue: A small hole may be present in the inner tray of specific lots of sterile...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 4, 2016· Zimmer Manufacturing B.V.

Recalled Item: Herbert Cannulated Bone Screw System Recalled by Zimmer Manufacturing B.V....

The Issue: A small hole may be present in the inner tray of specific lots of sterile...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 4, 2016· Cordis Corporation

Recalled Item: Cordis PRECISE (R) RX Nitinol Stent System (Biliary) Recalled by Cordis...

The Issue: Inability to deploy the stent or partial stent deployment.

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 4, 2016· Zimmer Manufacturing B.V.

Recalled Item: Zimmer Plates and Screws (ZPS) 2.7 mm Cortical Screw SelfTapping Recalled by...

The Issue: A small hole may be present in the inner tray of specific lots of sterile...

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

Class II — Potential Health HazardOngoing