Recall Z-0102-2018— Zimmer Biomet, Inc.

Name: FDA recall Z-0102-2018
Creator: U.S. Food and Drug Administration
Published: 2014-02-14

Class II · Terminated

Class II FDA medical device recall by Zimmer Biomet, Inc., initiated 2014-02-14, terminated 2020-09-16. It names 2 FDA 510(k) clearances: K101791, K092239. Product: ROSA Surgical Device 2.5.8. It is intended to be used in the operating room for the spatial positioning and orientation of an instrument holder or tool guide. Reason: An undetected shift between the information displayed in the navigation software and the actual patient anatomy.

Recalling firm: Zimmer Biomet, Inc.
Classification: Class II
Status: Terminated
Initiated: 2014-02-14
Terminated: 2020-09-16
Firm location: Warsaw, IN, United States

510(k) clearances named in this recall

2 on FDA's record

K101791 — ROSA SURGICAL DEVICEMedtech S.A.S·cleared 2010-09-23
K092239 — ROSA SURGICAL DEVICE, MODEL ROSA 1.1Medtech S.A·cleared 2009-11-17

K-numbers as listed on FDA's Recall Enterprise System record for this event (openFDA device/recall k_numbers). The recall may also cover devices cleared under other submissions not named here.

Product description

ROSA Surgical Device 2.5.8. It is intended to be used in the operating room for the spatial positioning and orientation of an instrument holder or tool guide

Reason for recall

An undetected shift between the information displayed in the navigation software and the actual patient anatomy

Data sourced from openFDA. This site is unofficial and independent of the FDA.