NuVasive Inc: Medical Device Recall in 2012 - (Recall #: Z-0360-2013)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2012.

Data Source: FDA.

Product Description:

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

Product Classification:

Class II

Date Initiated: January 5, 2009

Date Posted: November 28, 2012

Recall Number: Z-0360-2013

Event ID: 52634

Reason for Recall:

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

Status: Terminated

Product Quantity: 240 units total

Code Information:

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

Distribution Pattern:

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

Voluntary or Mandated:

Voluntary: Firm initiated