Reported Nov 13, 2019 · Terminated

Cephalomedullary Nail (CMN), Various sizes, Item Nos. 47249318009 47249318010 47249318011 47249318013 47249318014…

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?

  • Cephalomedullary Nail (CMN), Various sizes, Item Nos.

    224 of 224 codes

    • 47249318009
    • 47249318010
    • 47249318011
    • 47249318013
    • 47249318014
    • 47249318109
    • 47249318110
    • 47249318111
    • 47249318113
    • 47249318114
    • 47249318209
    • 47249318210
    • 47249318211
    • 47249318213
    • 47249318214
    • 47249318309
    • 47249318310
    • 47249318311
    • 47249318313
    • 47249318314
    • 47249321010
    • 47249321011
    • 47249321013
    • 47249321014
    • 47249321110
    • 47249321111
    • 47249321113
    • 47249321114
    • 47249321210
    • 47249321211
    • 47249321213
    • 47249321214
    • 47249321310
    • 47249321311
    • 47249321313
    • 47249321314
    • 47249321410
    • 47249321411
    • 47249321413
    • 47249321414
    • 47249321510
    • 47249321511
    • 47249321513
    • 47249321514
    • 47249330010
    • 47249330011
    • 47249330013
    • 47249330110
    • 47249330111
    • 47249330113
    • 47249330210
    • 47249330211
    • 47249330213
    • 47249330310
    • 47249330311
    • 47249330313
    • 47249330410
    • 47249330411
    • 47249330413
    • 47249330510
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, 6:06 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.