Class III — Low Risk

Low risk — use of or exposure to this product is not likely to cause adverse health consequences.

Ascension Modular Radial Head (MRH) Radial Head Implant Recalled by Ascension Orthopedics, Inc Due to The product was packaged with the Instructions for...

Date: November 16, 2018
Company: Ascension Orthopedics, 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 Ascension Orthopedics, Inc directly.

Affected Products

Ascension Modular Radial Head (MRH) Radial Head Implant, Catalog Number, MRH-350-04-WW

Why Was This Recalled?

The product was packaged with the Instructions for Use for a different product (Ascension First Choice DRUJ System Partial Ulnar Head Implant).

Where Was This Sold?

This product was distributed to 1 state: MO

Affected (1 state)Not affected

About Ascension Orthopedics, Inc

Ascension Orthopedics, Inc has 1 total recall tracked by RecallDetector.

Related Recalls

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