Reported Nov 13, 2019 · Terminated

Various Devices for Limb salvage arthroplasty, Item Nos. 00585000011 00585001201 00585001202 00585001301 00585001302…

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 Devices for Limb salvage arthroplasty, Item Nos.

    93 of 93 codes

    • 00585000011
    • 00585001201
    • 00585001202
    • 00585001301
    • 00585001302
    • 00585003038
    • 00585003214
    • 00585003217
    • 00585003219
    • 00585003238
    • 00585003246
    • 00585004445
    • 00585004455
    • 00585004465
    • 00585004603
    • 00585004604
    • 00585004605
    • 00585004606
    • 00585004608
    • 00585004610
    • 00585004612
    • 00585004614
    • 00585004616
    • 00585004618
    • 00585004620
    • 00585004622
    • 00585004635
    • 00585004645
    • 00585004655
    • 00585004808
    • 00585004809
    • 00585004820
    • 00585204209
    • 00585204217
    • 00585205009
    • 00585205010
    • 00585205011
    • 00585205012
    • 00585205013
    • 00585205014
    • 00585205015
    • 00585205016
    • 00585205017
    • 00585205018
    • 00585205019
    • 00585205209
    • 00585205210
    • 00585205211
    • 00585205212
    • 00585205213
    • 00585205214
    • 00585205215
    • 00585205216
    • 00585205217
    • 00585205218
    • 00585205219
    • 00585205412
    • 00585205413
    • 00585205414
    • 00585205415
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, 4:51 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.