Class II — Potential Health Hazard

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

Vision RingLoc Shell 50 mm Size 23. Hip joint replacement prosthesis. Recalled by Biomet, Inc. Due to The device was assembled without screw hole plugs.

Date: July 28, 2015
Company: Biomet, 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 Biomet, Inc. directly.

Affected Products

Vision RingLoc Shell 50 mm Size 23. Hip joint replacement prosthesis.

Quantity: 5

Why Was This Recalled?

The device was assembled without screw hole plugs.

Where Was This Sold?

Distributed in Canada and Japan.

About Biomet, Inc.

Biomet, Inc. has 250 total recalls tracked by RecallDetector.

Related Recalls

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