Class II — Potential Health Hazard

Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.

6.5mm x 45mm Noncannulated Screw Shank Subsequent Codes: KWP Recalled by NuVasive Inc Due to The tulip portion of the screw assembly can...

Date: January 5, 2009
Company: NuVasive Inc
Status: Terminated
Source: FDA (Device)

What You Should Do

Stop using this product immediately. Do not consume, use, or distribute it.

Return the product to the place of purchase for a full refund. If you have questions, contact NuVasive Inc directly.

Affected Products

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

Quantity: 240 units total

Why Was This Recalled?

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

Where Was This Sold?

This product was distributed nationwide across all 50 states.

Affected (51 states)Not affected

About NuVasive Inc

NuVasive Inc has 36 total recalls tracked by RecallDetector.

Related Recalls

Data sourced from the FDA (Device). Last updated March 26, 2026. View original report