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 Partial Knee System Recalled by Zimmer Biomet, Inc. Due to Finishing guide does not adequately account for shape...

Date: July 5, 2017
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 Partial Knee System, Size 8, Finishing Guide

Quantity: 158 devices

Why Was This Recalled?

Finishing guide does not adequately account for shape differences present in Size 8 of Persona Partial Knee System, potentially resulting in additional surgery time or sensation of tightness during knee flexion.

Where Was This Sold?

This product was distributed to 16 states: AZ, CA, CO, ID, IL, IN, MD, MA, MI, NJ, NM, PA, SC, TX, WA, WI

Affected (16 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