Zimmer Biomet, Inc.: Medical Device Recall in 2017 - (Recall #: Z-0116-2018)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2017.

Data Source: FDA.

Product Description:

ROSA BRAIN 3.0.0

Product Classification:

Class II

Date Initiated: July 29, 2016

Date Posted: November 29, 2017

Recall Number: Z-0116-2018

Event ID: 77741

Reason for Recall:

Non-conforming product label.

Status: Terminated

Product Quantity: 2 devices

Code Information:

Serial No. BR16017 and BR16018

Distribution Pattern:

OH and PA.

Voluntary or Mandated:

Voluntary: Firm initiated