Reported Jun 15, 2016 · Terminated

Persona Trabecular Metal Tibia; Persona Trabecular Metal Tibial Plate Instruments and Modular Brackets; Used to…

Zimmer Biomet, Inc.

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

What you should do

Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.

Firm contact: Zimmer Biomet, Inc. · 1800 W Center St · Warsaw, IN · 46580-2304

Is this the product you have?

Persona Trabecular Metal Tibia; Persona Trabecular Metal Tibial Plate Instruments and Modular Brackets; Used to facilitate the implantation of joint replacement implants.

Lot codes and dates: Part Number, Lot Number
Date of Manufacture
669 of 669 codes
42509909210
63138589
07/28/2015
42509909210
63097616
06/10/2015
00590708181
56595825
04/20/2015
00590708185
56610423
03/12/2015
00590708176
56595826
03/04/2015
00590708179
56595827
03/04/2015
00590708180
56595828
03/04/2015
00590708181
56595824
03/02/2015
00590708178
56595692
02/17/2015
00590708176
56595691
02/16/2015
00590708177
56595801
02/16/2015
00590708180
56595694
02/04/2015
00590708179
56595693
01/29/2015
00590708181
56595642
01/20/2015
00590708177
56595625
01/06/2015
42539807902
62906456
12/14/2014
00590708178
56595569
12/12/2014
42539808802
62885379
11/22/2014
42539807102
62885377
11/21/2014
42539806702
62885376
11/20/2014
Amount recalled: 10,256

Where it was sold

Why it was recalled

Zimmer Inc. is initiating a recall of specific Persona" Trabecular Metal" Tibial Plate Instruments and Modular Brackets, due to incidents of radiolucent lines and loosening in implants.

This product could cause temporary or reversible health problems — stop using it.

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By hazard

Medical device recalls

Other recalls from Zimmer Biomet, Inc.

84 in total.

Where it was distributed

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