Zimmer Biomet, Inc.: Medical Device Recall in 2017 - (Recall #: Z-0178-2018)

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 Surgical Device 2.5.8

Product Classification:

Class II

Date Initiated: February 10, 2013

Date Posted: December 6, 2017

Recall Number: Z-0178-2018

Event ID: 77672

Reason for Recall:

Issue with optional neuro-endoscopy module detected under specific conditions during internal testing.

Status: Terminated

Product Quantity: 22 units (4 US and 18 OUS)

Code Information:

Serial No. RO10011, RO10014, RO13023 and RO13027

Distribution Pattern:

AR, OH, MI, and TX

Voluntary or Mandated:

Voluntary: Firm initiated