Z-1171-2017 Class II Terminated

Recalled by Biomet U.K., Ltd. — Bridgend South Wales, N/A

Recall Details

Product Type
Devices
Report Date
March 1, 2017
Initiation Date
January 5, 2016
Termination Date
June 30, 2018
Voluntary/Mandated
Voluntary: Firm initiated
Product Quantity
72 units in total

Product Description

Oxford Partial Knee System Phase 3 Tibial Template Right Medial Size D Product Usage: Instruments for use with the Oxford Uni Partial Knee System

Reason for Recall

Zimmer Biomet is conducting a medical device field action for various lot-specific Oxford Knee instruments due to potential alumina inclusions in the raw material batch used to produce the affected products. Inclusions contained within the finished product could lead to the cracking and separation of the instrument.

Distribution Pattern

Worldwide Distribution in the states of LA, NC, AR, MT, MO, CA, NY, KS, TX, MA, KY, OK, SC, NJ and the countries of Foreign: THAILAND, JAPAN, NETHERLANDS

Code Information

Item:32-420060, Lots: ZB160701