PlainRecalls
FDA Devices Moderate Class II Terminated

ROSA BRAIN 3.0.0

Reported: November 29, 2017 Initiated: July 29, 2016 #Z-0116-2018

Product Description

ROSA BRAIN 3.0.0

Reason for Recall

Non-conforming product label.

Details

Recalling Firm
Zimmer Biomet, Inc.
Units Affected
2 devices
Distribution
OH and PA.
Location
Warsaw, IN

Frequently Asked Questions

What product was recalled?
ROSA BRAIN 3.0.0. Recalled by Zimmer Biomet, Inc.. Units affected: 2 devices.
Why was this product recalled?
Non-conforming product label.
Which agency issued this recall?
This recall was issued by the FDA Devices on November 29, 2017. Severity: Moderate. Recall number: Z-0116-2018.