Reported Nov 13, 2019 · Terminated

Universal Locking Plates Sterile, Item Nos. 47492800207 47492800303 47492800402 47492800403 47492800407 47492800502…

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?

  • Universal Locking Plates Sterile, Item Nos.

    113 of 113 codes

    • 47492800207
    • 47492800303
    • 47492800402
    • 47492800403
    • 47492800407
    • 47492800502
    • 47492800503
    • 47492800507
    • 47492800603
    • 47492800607
    • 47492800613
    • 47492800702
    • 47492800703
    • 47492800707
    • 47492800802
    • 47492800803
    • 47492800807
    • 47492800813
    • 47492800902
    • 47492800907
    • 47492801002
    • 47492801007
    • 47492801013
    • 47492801207
    • 47492801213
    • 47492801413
    • 47492801607
    • 47492801613
    • 47492801702
    • 47492801802
    • 47492801813
    • 47492801902
    • 47492802002
    • 47492802013
    • 47493600313
    • 47493600403
    • 47493600407
    • 47493600413
    • 47493600503
    • 47493600507
    • 47493600513
    • 47493600603
    • 47493600607
    • 47493600613
    • 47493600703
    • 47493600707
    • 47493600713
    • 47493600803
    • 47493600807
    • 47493600813
    • 47493600907
    • 47493600913
    • 47493601003
    • 47493601007
    • 47493601013
    • 47493601113
    • 47493601203
    • 47493601207
    • 47493601213
    • 47493601313
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, 5:34 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.