Z-0993-2018 Class II Terminated

Recalled by Zimmer Biomet, Inc. — Warsaw, IN

FDA device recall Z-0993-2018 was initiated by Zimmer Biomet, Inc. on June 30, 2017 and is designated Class II. Reason for recall: For soft tissue fixation The recall status is terminated (terminated April 13, 2018). Affected quantity: 50.

Recall Details

Product Type
Devices
Report Date
March 21, 2018
Initiation Date
June 30, 2017
Termination Date
April 13, 2018
Voluntary/Mandated
Voluntary: Firm initiated
Product Quantity
50

Product Description

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

Reason for Recall

For soft tissue fixation

Distribution Pattern

US in the state of Texas

Code Information

Part number: 912050 Lot number: 221890