Recall Z-1684-2016— Zimmer Manufacturing B.V.

Name: FDA recall Z-1684-2016
Creator: U.S. Food and Drug Administration
Published: 2016-05-04

Class II · Terminated

Class II FDA medical device recall by Zimmer Manufacturing B.V., initiated 2016-05-04, terminated 2017-07-05. It names one FDA 510(k) clearance: K934765. Product: Trilogy self-tapping bone screw Bone screw 4.5x25 selftap 00625004525 Bone screw 4.5x50 selftap 00625004550 Bone screw 6.5x15 selftap 00625006515 Bone screw 6.5x20 selftap 00625006520 Bone screw 6.5x25 selftap 00625006525 Bone screw 6.5x30 selftap 00625006530. Reason: A small hole may be present in the inner tray of specific lots of sterile Hip and Trauma Implant Screws..

Recalling firm: Zimmer Manufacturing B.V.
Classification: Class II
Status: Terminated
Initiated: 2016-05-04
Terminated: 2017-07-05
Firm location: Mercedita, PR, United States

510(k) clearances named in this recall

1 on FDA's record

K934765 — TRILOGY ACETABULAR SYSTEMZimmer, Inc.·cleared 1994-04-29

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

Trilogy self-tapping bone screw Bone screw 4.5x25 selftap 00625004525 Bone screw 4.5x50 selftap 00625004550 Bone screw 6.5x15 selftap 00625006515 Bone screw 6.5x20 selftap 00625006520 Bone screw 6.5x25 selftap 00625006525 Bone screw 6.5x30 selftap 00625006530

Reason for recall

A small hole may be present in the inner tray of specific lots of sterile Hip and Trauma Implant Screws.

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