Reported Nov 13, 2019 · Terminated

Various Hip Joint Replacement Systems, Item Nos. 00151504232 00151504432 00151504636 00151504836 00151505040…

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 Hip Joint Replacement Systems, Item Nos.

    304 of 304 codes

    • 00151504232
    • 00151504432
    • 00151504636
    • 00151504836
    • 00151505040
    • 00151505240
    • 00151505444
    • 00151505644
    • 00151505848
    • 00151506048
    • 00151506248
    • 00151506448
    • 00151506648
    • 00400500060
    • 00401000038
    • 00401000040
    • 00401000041
    • 00401000042
    • 00401000043
    • 00401000044
    • 00401000045
    • 00401000046
    • 00401000047
    • 00401000048
    • 00401000049
    • 00401000050
    • 00401000051
    • 00401000052
    • 00401000053
    • 00401000054
    • 00401000055
    • 00402100857
    • 00402100863
    • 00402101243
    • 00402101244
    • 00402200040
    • 00402200042
    • 00402200051
    • 00402200057
    • 00408801106
    • 00408801206
    • 00408801226
    • 00408801236
    • 00408801306
    • 00408801326
    • 00408801336
    • 00408801356
    • 00408801376
    • 00408801406
    • 00408801426
    • 00408801436
    • 00408801456
    • 00408801476
    • 00408801506
    • 00408801526
    • 00408801536
    • 00408801556
    • 00408801576
    • 00408801606
    • 00408801626
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, 4:45 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.