Recall Z-2365-2018— Zimmer Biomet, Inc.

Name: FDA recall Z-2365-2018
Creator: U.S. Food and Drug Administration
Published: 2018-05-30

Class II · Terminated

Class II FDA medical device recall by Zimmer Biomet, Inc., initiated 2018-05-30, terminated 2020-05-28. It names one FDA 510(k) clearance: K063251. Product: Zimmer¿ M/L Taper Hip Prosthesis With Kinective¿ Technology Cementless, Size 10; 00-7713-010-00.

Recalling firm: Zimmer Biomet, Inc.
Classification: Class II
Status: Terminated
Initiated: 2018-05-30
Terminated: 2020-05-28
Firm location: Warsaw, IN, United States

510(k) clearances named in this recall

1 on FDA's record

K063251 — ZIMMER M/L TAPER HIP PROSTHESIS WITH MODULAR NECK TECHNOLOGYZimmer, Inc.·cleared 2007-01-24

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

Zimmer¿ M/L Taper Hip Prosthesis With Kinective¿ Technology Cementless, Size 10; 00-7713-010-00

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