Reported Nov 13, 2019 · Terminated

Various Knee Systems for knee joint arthroplasty, knee prosthesis, Item Nos. 00522000100 00522000200 00522000300…

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?

  • Various Knee Systems for knee joint arthroplasty, knee prosthesis, Item Nos.

    302 of 302 codes

    • 00522000100
    • 00522000200
    • 00522000300
    • 00522000400
    • 00522006304
    • 00522006504
    • 00522006600
    • 00522006800
    • 00522006900
    • 00522007000
    • 00522007200
    • 00522007300
    • 00522007400
    • 00522007500
    • 00522007900
    • 00522008000
    • 00522400800
    • 00522400900
    • 00522406201
    • 00541001401
    • 00541001501
    • 00541001502
    • 00541001601
    • 00541001602
    • 00541001701
    • 00541001702
    • 00541001801
    • 00541001802
    • 00541201501
    • 00541201502
    • 00541201601
    • 00541201602
    • 00541201701
    • 00541201702
    • 00541201801
    • 00541201802
    • 00541401301
    • 00541401302
    • 00541401401
    • 00541401402
    • 00541401501
    • 00541401502
    • 00541401601
    • 00541401602
    • 00541401701
    • 00541401702
    • 00541601401
    • 00541601402
    • 00541601501
    • 00541601502
    • 00541601601
    • 00541601602
    • 00575001301
    • 00575001302
    • 00575001305
    • 00575001306
    • 00575001401
    • 00575001402
    • 00575001405
    • 00575001406
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.

Want the full recall guide?

The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.

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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, 5:38 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.