Class II — Potential Health Hazard

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

IO Fix IntraOsseous Fixation System Recalled by Extremity Medical LLC Due to Product Event Reports revealed that lag screw passes...

Date: April 13, 2011
Company: Extremity Medical 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 Extremity Medical LLC directly.

Affected Products

IO Fix IntraOsseous Fixation System; Extremity Medical. www.extremitymedical.com; Customer Service: 888.499.0079. The Extremity Medical Screw and Washer System is intended for reduction and internal fixation of arthrodeses, osteotomies, intra- and extrarticular fractures and nonunions of the small bones and joints of the foot, ankle, hand and wrist.

Quantity: 120 Units

Why Was This Recalled?

Product Event Reports revealed that lag screw passes through washer (e.g. X-Post) intra-operatively.

Where Was This Sold?

This product was distributed nationwide across all 50 states.

Affected (51 states)Not affected

About Extremity Medical LLC

Extremity Medical LLC has 4 total recalls tracked by RecallDetector.

Related Recalls

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