Class II — Potential Health Hazard

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

ROSA Surgical Device 2.5.8 Recalled by Zimmer Biomet, Inc. Due to Potential failure of a force feedback sensor that...

Date: November 6, 2014
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

ROSA Surgical Device 2.5.8, a computer-controlled electromechanical arm to guide standard neurosurgical instruments.

Quantity: 31 units

Why Was This Recalled?

Potential failure of a force feedback sensor that may result in continued movement of an operating arm (rather than an immediate stop as intended).

Where Was This Sold?

This product was distributed to 5 states: AR, GA, MI, OH, TX

Affected (5 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