Reported Nov 13, 2019 · Terminated

Various fixation systems and accessories, Item Nos. 00224000916 00224000918 00224000920 00224000922 00224000924…

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 fixation systems and accessories, Item Nos.

    304 of 304 codes

    • 00224000916
    • 00224000918
    • 00224000920
    • 00224000922
    • 00224000924
    • 00224000926
    • 00224000928
    • 00224000930
    • 00224000932
    • 00224000934
    • 00224000936
    • 00224000938
    • 00224000940
    • 00224000942
    • 00224000944
    • 00224000946
    • 00224001014
    • 00224001016
    • 00224001018
    • 00224001020
    • 00224001022
    • 00224001024
    • 00224001026
    • 00224001028
    • 00224001030
    • 00224001032
    • 00224001034
    • 00224001036
    • 00224001038
    • 00224001040
    • 00224001042
    • 00224001046
    • 00224001048
    • 00224001114
    • 00224001116
    • 00224001118
    • 00224001120
    • 00224001122
    • 00224001124
    • 00224001126
    • 00224001128
    • 00224001130
    • 00224001132
    • 00224001134
    • 00224001136
    • 00224001138
    • 00224001140
    • 00224001142
    • 00224001144
    • 00224001146
    • 00224001214
    • 00224001216
    • 00224001218
    • 00224001220
    • 00224001222
    • 00224001224
    • 00224001226
    • 00224001228
    • 00224001230
    • 00224001232
Lot codes and dates
  • All products 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, 4:50 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.