Class II — Potential Health Hazard

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

Persona Trabecular Metal Tibia Recalled by Zimmer Biomet, Inc. Due to Zimmer Inc. is initiating a recall of specific...

Date: May 11, 2016
Company: Zimmer 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 Zimmer Biomet, Inc. directly.

Affected Products

Persona Trabecular Metal Tibia; Persona Trabecular Metal Tibial Plate Instruments and Modular Brackets; Used to facilitate the implantation of joint replacement implants.

Quantity: 10,256

Why Was This Recalled?

Zimmer Inc. is initiating a recall of specific Persona" Trabecular Metal" Tibial Plate Instruments and Modular Brackets, due to incidents of radiolucent lines and loosening in implants.

Where Was This Sold?

This product was distributed to 30 states: AL, AK, AZ, CA, FL, GA, HI, ID, IL, IN, KS, KY, MD, MA, MI, MN, MO, NJ, NY, NC, OH, OK, PA, SC, TN, TX, UT, VA, WA, WI

Affected (30 states)Not affected

About Zimmer Biomet, Inc.

Zimmer Biomet, Inc. has 875 total recalls tracked by RecallDetector.

Related Recalls

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