Class II — Potential Health Hazard

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

Endoskeleton" TAS Interbody System with Titan nanoLOCK" Surface Technology Recalled by Medtronic Sofamor Danek USA Inc Due to Engraving on implants may not match what is...

Date: September 2, 2021
Company: Medtronic Sofamor Danek USA 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 Medtronic Sofamor Danek USA Inc directly.

Affected Products

Endoskeleton" TAS Interbody System with Titan nanoLOCK" Surface Technology, Nanolock 12 Dg Interbody, Large, 12mm

Quantity: 10 units

Why Was This Recalled?

Engraving on implants may not match what is listed on the pouch labels.

Where Was This Sold?

This product was distributed to 14 states: CA, MN, MO, NV, NY, NC, OH, OK, OR, PA, SC, SD, WA, WV

Affected (14 states)Not affected

About Medtronic Sofamor Danek USA Inc

Medtronic Sofamor Danek USA Inc has 81 total recalls tracked by RecallDetector.

Related Recalls

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