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 2096120980 of 29,737 recalls

Medical DeviceMay 4, 2016· Zimmer Manufacturing B.V.

Recalled Item: ITST intertrochanteric/subtrochanteric fixation 4.5 mm diameter cortical...

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: Trilogy self-tapping bone screw Bone screw 4.5x25 selftap 00625004525 Bone...

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: M/DN Intramedullary Fixation 4.2 mm Diameter Cortical Screw 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: Zimmer Plates and Screws (ZPS) 4.0 mm Cancellous Screw Fully Threaded...

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: Hgp ii acetabular cup bone screw selftap 6.5x15mm 00662406515 Hgp Recalled...

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: VersaFx Femoral Fixation System Hex head compression screw 4.7 mm Recalled...

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: Mini MagnaFx Cannulated Screw Fixation System Small Cannulated Bone Screw...

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: Periarticular plating system Recalled by Zimmer Manufacturing B.V. Due to A...

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) PRO RX Nitinol Stent System (Carotid) 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 2, 2016· Synthes (USA) Products LLC

Recalled Item: 1.5 mm Rapid Resorb Orbt1 F1 P1 w/Bending Template / 30 mm - Sterile...

The Issue: Labeling errors. The outer packge label expiration date may exceed the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 2, 2016· Leica Biosystems Richmond Inc.

Recalled Item: CytoVision Image Analysis and Capture System Recalled by Leica Biosystems...

The Issue: Systems have an improperly activated Windows 7 OS, even though a valid...

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

Class III — Low RiskOngoing
Medical DeviceMay 2, 2016· Synthes (USA) Products LLC

Recalled Item: 1.5 mm Rapid Resorb Orbt1 F1 P1 w/Bending Template / 35 mm - Sterile...

The Issue: Labeling errors. The outer packge label expiration date may exceed the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 2, 2016· Synthes (USA) Products LLC

Recalled Item: 1.5 mm Rapid Resorb Orbt1 F1 P1 w/Bending Template / 24 mm - Sterile...

The Issue: Labeling errors. The outer packge label expiration date may exceed the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 2, 2016· Synthes (USA) Products LLC

Recalled Item: DePuy Synthes 8.0 mm Flexible Shaft Reamer Recalled by Synthes (USA)...

The Issue: Devices did not pass the biological safety evaluation for cytotoxicity...

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

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

Recalled Item: Siemens Healthcare ADVIA Centaur Tnl-Ultra Assay . In-Vitro Diagnostic for...

The Issue: Exhibits a greater than 10% change in results in samples with biotin levels...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 29, 2016· Philips Medical Systems (Cleveland) Inc

Recalled Item: Brilliance 64 CT Model 728231 Recalled by Philips Medical Systems...

The Issue: Software issues found in software versions v4.1.3/4.1.4/4.1.5 in the Philips...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 29, 2016· Philips Medical Systems (Cleveland) Inc

Recalled Item: Ingenuity CT Model No. 728326 Recalled by Philips Medical Systems...

The Issue: Software issues in v4.1.3/4.1.4/4.1.5 in the Philips Ingenuity CT products...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 29, 2016· Integra LifeSciences Corp.

Recalled Item: Cadence Size 5 Left Tibial Tray Implant Recalled by Integra LifeSciences...

The Issue: As a result of an internal review of all labeling for the Cadence System, it...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 29, 2016· Philips Medical Systems (Cleveland) Inc

Recalled Item: Brilliance iCT SP Model No. 728311 Recalled by Philips Medical Systems...

The Issue: Software issues found in v4.1 .3/4.1.5 in the Philips Brilliance iCT/ iCT SP...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 29, 2016· Philips Medical Systems (Cleveland) Inc

Recalled Item: Ingenuity Core128 Model No. 728323 Recalled by Philips Medical Systems...

The Issue: Software issues in v4.1.3/4.1.4/4.1.5 in the Philips Ingenuity CT products...

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

Class II — Potential Health HazardOngoing