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 Brain 3.0 Stereotaxic instrument Computer-assisted surgical device. Intended for Recalled by Zimmer Biomet, Inc. Due to Robot arm being sent to the wrong position

Date: May 1, 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

ROSA Brain 3.0 Stereotaxic instrument Computer-assisted surgical device. Intended for the spatial positioning and orientation of instrument holders to be used by neurosurgeons.

Quantity: 16

Why Was This Recalled?

Robot arm being sent to the wrong position

Where Was This Sold?

This product was distributed to 11 states: CA, FL, IL, KY, MA, MN, NY, NC, OH, PA, DC

Affected (11 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