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. 1,887 recalls have been distributed to North Carolina in the last 12 months.

54,363 total recalls
1,887 in last 12 months

Showing 2866128680 of 29,737 recalls

Medical DeviceSeptember 4, 2012· Zimmer, Inc.

Recalled Item: Fitmore" Hip Stem Recalled by Zimmer, Inc. Due to Zimmer Inc., is initiating...

The Issue: Zimmer Inc., is initiating a correction to the patient labels of products...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 4, 2012· Zimmer, Inc.

Recalled Item: Anatomical Shoulder" Revision Humeral stem Recalled by Zimmer, Inc. Due to...

The Issue: Zimmer Inc., is initiating a correction to the patient labels of products...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 4, 2012· Zimmer, Inc.

Recalled Item: Dynesys¿ HA Pedicle + set screw Recalled by Zimmer, Inc. Due to Zimmer Inc.,...

The Issue: Zimmer Inc., is initiating a correction to the patient labels of products...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 4, 2012· Zimmer, Inc.

Recalled Item: CLS Stem Recalled by Zimmer, Inc. Due to Zimmer Inc., is initiating a...

The Issue: Zimmer Inc., is initiating a correction to the patient labels of products...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 4, 2012· Davol, Inc., Subs. C. R. Bard, Inc.

Recalled Item: Bard Ventralight ST Mesh. - Ellipse 8" x 10" (20.3 Recalled by Davol, Inc.,...

The Issue: Mislabeled: The 8" x 10" package contains 7" x 9" VENTRALIGHT ST Mesh...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 4, 2012· Zimmer, Inc.

Recalled Item: MS-30¿ Proximal positioner Recalled by Zimmer, Inc. Due to Zimmer Inc., is...

The Issue: Zimmer Inc., is initiating a correction to the patient labels of products...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 4, 2012· Zimmer, Inc.

Recalled Item: Anatomical Shoulder" Fracture Humeral stem Recalled by Zimmer, Inc. Due to...

The Issue: Zimmer Inc., is initiating a correction to the patient labels of products...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 4, 2012· Zimmer, Inc.

Recalled Item: NCB¿-PH Plate Recalled by Zimmer, Inc. Due to Zimmer Inc., is initiating a...

The Issue: Zimmer Inc., is initiating a correction to the patient labels of products...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 4, 2012· Zimmer, Inc.

Recalled Item: Zimmer Inverse/Reverse Screw system Recalled by Zimmer, Inc. Due to Zimmer...

The Issue: Zimmer Inc., is initiating a correction to the patient labels of products...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 4, 2012· Zimmer, Inc.

Recalled Item: Metasul¿ Durom¿ Femoral component Sterile Recalled by Zimmer, Inc. Due to...

The Issue: Zimmer Inc., is initiating a correction to the patient labels of products...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 4, 2012· Zimmer, Inc.

Recalled Item: Anatomical Shoulder" Fracture Humeral Head Recalled by Zimmer, Inc. Due to...

The Issue: Zimmer Inc., is initiating a correction to the patient labels of products...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 4, 2012· Zimmer, Inc.

Recalled Item: Dynesys¿ Set screw M6 Recalled by Zimmer, Inc. Due to Zimmer Inc., is...

The Issue: Zimmer Inc., is initiating a correction to the patient labels of products...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 4, 2012· Zimmer, Inc.

Recalled Item: Dynesys¿ Universal spacer 6-45 Recalled by Zimmer, Inc. Due to Zimmer Inc.,...

The Issue: Zimmer Inc., is initiating a correction to the patient labels of products...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 4, 2012· Zimmer, Inc.

Recalled Item: NCB¿ screw ¿ 4.0 self-tapping Recalled by Zimmer, Inc. Due to Zimmer Inc.,...

The Issue: Zimmer Inc., is initiating a correction to the patient labels of products...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 4, 2012· Advanced Neuromodulation Systems Inc.

Recalled Item: The Eon Mini Implantable Pulse Generator (IPG) is a 16-channel Recalled by...

The Issue: Eon Mini IPGs manufactured in April 2012 could potentially exhibit a sudden,...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 4, 2012· Zimmer, Inc.

Recalled Item: CoCr Head Recalled by Zimmer, Inc. Due to Zimmer Inc., is initiating a...

The Issue: Zimmer Inc., is initiating a correction to the patient labels of products...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 4, 2012· Zimmer, Inc.

Recalled Item: Dynesys¿ Top-Loading System Cannulated Pedicle + Set Screw Recalled by...

The Issue: Zimmer Inc., is initiating a correction to the patient labels of products...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 4, 2012· Zimmer, Inc.

Recalled Item: Anatomical Shoulder" Ball taper for humeral stem Recalled by Zimmer, Inc....

The Issue: Zimmer Inc., is initiating a correction to the patient labels of products...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 4, 2012· Zimmer, Inc.

Recalled Item: Sirus¿ intramedullary nail for tibia Recalled by Zimmer, Inc. Due to Zimmer...

The Issue: Zimmer Inc., is initiating a correction to the patient labels of products...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 4, 2012· Zimmer, Inc.

Recalled Item: NCB¿-PT lateral proximal 3 hole tibial plate Recalled by Zimmer, Inc. Due to...

The Issue: Zimmer Inc., is initiating a correction to the patient labels of products...

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

Class II — Potential Health HazardOngoing