Class II — Potential Health Hazard

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

CoreLink LLC Recalled by CoreLink LLC Due to Specific lots of FLXfit implants have internal components...

Date: October 20, 2022
Company: CoreLink LLC
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 CoreLink LLC directly.

Affected Products

CoreLink LLC, FLXFIT 15, 32MM X 8MM, CAGE, REF: AT3208

Quantity: 18 units

Why Was This Recalled?

Specific lots of FLXfit implants have internal components that may have been manufactured using stainless steel rather than the specified titanium alloy.

Where Was This Sold?

This product was distributed nationwide across all 50 states.

Affected (51 states)Not affected

About CoreLink LLC

CoreLink LLC has 1 total recall tracked by RecallDetector.

Related Recalls

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