Recall Z-2520-2019— Zimmer Biomet, Inc.

Name: FDA recall Z-2520-2019
Creator: U.S. Food and Drug Administration
Published: 2019-08-15

Class II · Terminated

Class II FDA medical device recall by Zimmer Biomet, Inc., initiated 2019-08-15, terminated 2021-04-16. It names one FDA 510(k) clearance: K132873. Product: XP-XP Tibial Tray - Interlok 75 mm Item # 195757. Reason: The locking bar not fully engaging.

Recalling firm: Zimmer Biomet, Inc.
Classification: Class II
Status: Terminated
Initiated: 2019-08-15
Terminated: 2021-04-16
Firm location: Warsaw, IN, United States

510(k) clearances named in this recall

1 on FDA's record

K132873 — VANGUARD XP KNEE SYSTEMBiomet, Inc.·cleared 2013-12-11

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

XP-XP Tibial Tray - Interlok 75 mm Item # 195757

Reason for recall

The locking bar not fully engaging

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