Reported Nov 13, 2019 · Terminated

Various Knee Systems, Item Nos. 32855411838 32855411840 32855411842 32855411843 32855420307 32855420308 32855420309…

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 Knee Systems, Item Nos.

    186 of 186 codes

    • 32855411838
    • 32855411840
    • 32855411842
    • 32855411843
    • 32855420307
    • 32855420308
    • 32855420309
    • 32855420310
    • 32855420315
    • 32855430491
    • 32855430497
    • 32855430499
    • 32855430500
    • 32855430502
    • 32855430503
    • 32855430511
    • 32855430526
    • 32855430530
    • 32855430531
    • 32855430536
    • 32855430537
    • 32855430538
    • 32855430539
    • 32855430541
    • 32855430543
    • 32855430546
    • 32855430548
    • 32855430549
    • 32855430550
    • 32855430551
    • 32855430556
    • 32855430557
    • 32855430558
    • 32855430563
    • 32855430565
    • 32855430567
    • 32855430568
    • 32855430569
    • 32855430570
    • 32855430574
    • 32855430575
    • 32855430577
    • 32855450420
    • 32855450441
    • 32855450453
    • 32855450461
    • 32855450499
    • 32855470626
    • 32855470639
    • 32855470641
    • 32855470644
    • 32855470645
    • 32855470648
    • 32855470649
    • 32855470652
    • 32855470653
    • 32855470654
    • 32855470660
    • 32855470663
    • 32855470666
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.

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.

Free recall alerts

Get alerted about new Zimmer Biomet, Inc. recalls

One email when a matching recall is published. No account, no cost, unsubscribe in one click.

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.