6.5mm x 45mm Cannulated Screw Shank Subsequent Codes: KWP, KWQ, MNH, MNI

Recall Insight

This FDA Devices action (record #Z-0358-2013) was formally reported on November 28, 2012, with the manufacturer initiating the action on January 5, 2009. It is classified under Moderate severity (Class II), with a current status of Terminated. NuVasive Inc is listed as the recalling firm, operating out of San Diego, CA. Federal records indicate 240 units total units are affected.

The documented reason for this recall is: The tulip portion of the screw assembly can disengage from the shank after implantation. Distribution data in the federal record shows the product reached: Nationwide Distribution-including the states of OR, MO, FL, WI, CA, and NC.. Distribution scope directly affects the consumer exposure window and determines whether a recall remains regional or escalates into a nationwide advisory.

To put this record in context, PlainRecalls indexes 83,949 recalls across the FDA, CPSC, NHTSA and USDA FSIS going back to 1995. Within the same product category, the database holds 6 closely related recalls, of which 6 were also issued by FDA Devices. That clustering is a signal — repeated actions in a narrow category often indicate a systemic quality-control issue, a supplier-wide contamination, or a design defect that has propagated across product lines. This recall is roughly 14 years old; older recalls can remain relevant because many units enter resale, rental, and secondary-market channels where the original warning never reaches the end user. Always cross-check the recall number against the official agency page before relying on any summary.