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. 1,900 recalls have been distributed to North Carolina in the last 12 months.

54,363 total recalls
1,900 in last 12 months

Showing 2722127240 of 29,737 recalls

Medical DeviceJune 7, 2013· Baxter Healthcare Corp.

Recalled Item: Brand Name: SV Elastomeric Infusion Device. Indicated for the intravenous...

The Issue: Baxter Healthcare Corporation (Baxter) is issuing an Urgent Product Recall...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 7, 2013· Baxter Healthcare Corp.

Recalled Item: Brand Name: Coiled Tube Infusors (Portable Elastomeric Infusion Systems)....

The Issue: Due to an increase in complaints for leaks at the distal male Luer and Luer...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 7, 2013· Baxter Healthcare Corp.

Recalled Item: Brand Name: Intermate Infusion Pump. Indicated for the intravenous...

The Issue: Baxter Healthcare Corporation (Baxter) is issuing an Urgent Product Recall...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 7, 2013· Baxter Healthcare Corp.

Recalled Item: Brand Name: Regional Analgesia Infusor System with Patient Control....

The Issue: Baxter Healthcare Corporation (Baxter) is issuing an Urgent Product Recall...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 7, 2013· Baxter Healthcare Corp.

Recalled Item: Brand Name: Intermate Infusion Pump. Indicated for the intravenous...

The Issue: Baxter Healthcare Corporation (Baxter) is issuing an Urgent Product Recall...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 7, 2013· Biomet, Inc.

Recalled Item: Oxford Fixed Bearing Partial Knee Cemented Lateral Tibia Recalled by Biomet,...

The Issue: Biomet investigation found the design of the tibial bearing creates the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 7, 2013· Biomet, Inc.

Recalled Item: Oxford Fixed Bearing Partial Knee Cemented Lateral Tibia Recalled by Biomet,...

The Issue: Biomet investigation found the design of the tibial bearing creates the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 7, 2013· Biomet, Inc.

Recalled Item: Oxford Fixed Bearing Partial Knee Cemented Lateral Tibia Recalled by Biomet,...

The Issue: Biomet investigation found the design of the tibial bearing creates the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 7, 2013· Biomet, Inc.

Recalled Item: Oxford Fixed Bearing Partial Knee Cemented Lateral Tibia Recalled by Biomet,...

The Issue: Biomet investigation found the design of the tibial bearing creates the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 7, 2013· Codman & Shurtleff, Inc.

Recalled Item: MedStream Programmable Infusion Pump- Implantable for the intrathecal...

The Issue: Miscalibrated Fill Level Sensor may affect dosing level

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 7, 2013· Biomet, Inc.

Recalled Item: Oxford Fixed Bearing Partial Knee Cemented Lateral Tibia Recalled by Biomet,...

The Issue: Biomet investigation found the design of the tibial bearing creates the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 7, 2013· Codman & Shurtleff, Inc.

Recalled Item: MedStream Programmable Infusion Pump Recalled by Codman & Shurtleff, Inc....

The Issue: Miscalibrated Fill Level Sensor may affect dosing level

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 7, 2013· Biomet, Inc.

Recalled Item: Oxford Fixed Bearing Partial Knee Cemented Lateral Tibia Recalled by Biomet,...

The Issue: Biomet investigation found the design of the tibial bearing creates the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 7, 2013· Biomet, Inc.

Recalled Item: Fixed Bearing Partial Knee Cemented Lateral Tibia Size Recalled by Biomet,...

The Issue: Biomet investigation found the design of the tibial bearing creates the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 7, 2013· Biomet, Inc.

Recalled Item: Oxford Fixed Bearing Partial Knee Cemented Lateral Tibia Recalled by Biomet,...

The Issue: Biomet investigation found the design of the tibial bearing creates the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 7, 2013· Biomet, Inc.

Recalled Item: Oxford Fixed Bearing Partial Knee Cemented Lateral Tibia Recalled by Biomet,...

The Issue: Biomet investigation found the design of the tibial bearing creates the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 7, 2013· Biomet, Inc.

Recalled Item: Oxford Fixed Bearing Partial Knee Cemented Lateral Tibia Recalled by Biomet,...

The Issue: Biomet investigation found the design of the tibial bearing creates the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 7, 2013· Biomet, Inc.

Recalled Item: Oxford Fixed Bearing Partial Knee Cemented Lateral Tibia Recalled by Biomet,...

The Issue: Biomet investigation found the design of the tibial bearing creates the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 7, 2013· Biomet, Inc.

Recalled Item: Fixed Bearing Partial Knee Cemented Lateral Tibia Size Recalled by Biomet,...

The Issue: Biomet investigation found the design of the tibial bearing creates the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 7, 2013· Biomet, Inc.

Recalled Item: Oxford Fixed Bearing Partial Knee Cemented Lateral Tibia Recalled by Biomet,...

The Issue: Biomet investigation found the design of the tibial bearing creates the...

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

Class II — Potential Health HazardOngoing