Vehicle Safety Product Safety Food Safety Pet Safety Drug Safety Device Safety Workplace Safety Bridge Safety Aviation Safety Dam Safety Nursing Homes Water Safety Railroad Safety Pipeline Safety Environmental

6.5mm x 55mm Cannulated Screw Shank Subsequent Codes: KWP, KWQ, MNH, MNI

FDA Recall #Z-0360-2013 — Class II — January 5, 2009

Recall #Z-0360-2013 Date: January 5, 2009 Classification: Class II Status: Terminated

Product Description

6.5mm x 55mm Cannulated Screw Shank Subsequent Codes: KWP, KWQ, MNH, MNI

Reason for Recall

The tulip portion of the screw assembly can disengage from the shank after implantation.

Recalling Firm

NuVasive Inc — San Diego, CA

Classification

Class II — May cause temporary or medically reversible adverse health consequences.

Product Type

Devices

Product Quantity

240 units total

Distribution

Nationwide Distribution-including the states of OR, MO, FL, WI, CA, and NC.

Code Information

Batch: JK2060, JK2046, JK2180, JK2202, JK2213, JK2230, JK2231, JK2247, JK2244

Status

Terminated

Voluntary / Mandated

Voluntary: Firm initiated

Back to All Device Recalls