Reported Nov 13, 2019 · Terminated

Periarticular Plates - Tibial, Item Nos. 00234700304 00234700306 00234700308 00234700310 00234700312 00234700314…

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?

  • Periarticular Plates - Tibial, Item Nos.

    80 of 80 codes

    • 00234700304
    • 00234700306
    • 00234700308
    • 00234700310
    • 00234700312
    • 00234700314
    • 00234700316
    • 00234700404
    • 00234700406
    • 00234700408
    • 00234700410
    • 00234700412
    • 00234700414
    • 00234700416
    • 00234700502
    • 00234700504
    • 00234700506
    • 00234700508
    • 00234700510
    • 00234700512
    • 00234700514
    • 00234700602
    • 00234700604
    • 00234700606
    • 00234700608
    • 00234700610
    • 00234700612
    • 00234700614
    • 00234700704
    • 00234700706
    • 00234700708
    • 00234700710
    • 00234700712
    • 00234700714
    • 00234700716
    • 00234700718
    • 00234700720
    • 00234700804
    • 00234700806
    • 00234700808
    • 00234700810
    • 00234700812
    • 00234700814
    • 00234700816
    • 00234700818
    • 00234700820
    • 00234700904
    • 00234700906
    • 00234700908
    • 00234700910
    • 00234700912
    • 00234700914
    • 00234700916
    • 00234700918
    • 00234700920
    • 00234701004
    • 00234701006
    • 00234701008
    • 00234701010
    • 00234701012
Lot codes and dates
  • All product manufactured prior to January 2014.
Amount recalled
5,459,583 total devices

This recall covers 41 products

The agency filed one notice per product. You are reading one of them; the other 40 are below.

28 more are in the archive.

Where it was sold

  • Nationwide

Why it was recalled

Non-highly polished implants may adhere to the LDPE bag (previous packaging configuration).

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

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Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA device enforcement) notice

Notice updated May 19, 2020 · Data as of Sep 19, 6:15 PM UTC

RecallNow is not a government agency. Every fact on this page is published by the FDA, USDA or CPSC and links back to their notice.