Recall Z-0993-2018— Zimmer Biomet, Inc.

Name: FDA recall Z-0993-2018
Creator: U.S. Food and Drug Administration
Published: 2017-06-30

Class II · Terminated

Class II FDA medical device recall by Zimmer Biomet, Inc., initiated 2017-06-30, terminated 2018-04-13. It names one FDA 510(k) clearance: K131684. Product: JUGGERKNOT 2.9MM 2 #2 MB Product Usage: For use in hip arthroplasty. Reason: For soft tissue fixation.

Recalling firm: Zimmer Biomet, Inc.
Classification: Class II
Status: Terminated
Initiated: 2017-06-30
Terminated: 2018-04-13
Firm location: Warsaw, IN, United States

510(k) clearances named in this recall

1 on FDA's record

K131684 — BIOLOX(R) DELTA CERAMIC HEADSBiomet, Inc.·cleared 2013-10-10

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

JUGGERKNOT 2.9MM 2 #2 MB Product Usage: For use in hip arthroplasty

Reason for recall

For soft tissue fixation

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