Class II — Potential Health Hazard

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

Accolade and Restoration hip product Recalled by Howmedica Osteonics Corp. Due to Inner and outer sterile barriers not fully sealed.

Date: July 21, 2017
Company: Howmedica Osteonics Corp.
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 Howmedica Osteonics Corp. directly.

Affected Products

Accolade and Restoration hip product; Catalog Number: 6021-0030, 6276-1-127, 6276-5-216, 6020-2530, 6020-4535, 6021-0740, 6021-0230, and 6021-4535

Quantity: 255

Why Was This Recalled?

Inner and outer sterile barriers not fully sealed.

Where Was This Sold?

This product was distributed to 10 states: AR, DE, FL, IL, IN, MI, NJ, OH, TN, TX

Affected (10 states)Not affected

About Howmedica Osteonics Corp.

Howmedica Osteonics Corp. has 229 total recalls tracked by RecallDetector.

Related Recalls

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