Class II — Potential Health Hazard

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

Vanguard Knee System Series-A Standard Patella sizes 31mm Item Number: 184764 Recalled by Zimmer Biomet, Inc. Due to Vanguard Knee System Series-A Standard Patella a potential...

Date: December 21, 2018
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

Vanguard Knee System Series-A Standard Patella sizes 31mm Item Number: 184764

Quantity: 45 units

Why Was This Recalled?

Vanguard Knee System Series-A Standard Patella a potential commingle that could result in the size of the implant not matching the size on the label.

Where Was This Sold?

This product was distributed to 2 states: MN, VA

Affected (2 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