Reported Jun 17, 2015 · Terminated

MCK Maximum Congruent Knee System, BIOMET FINNED PRI STEM 40MM; 80 x 10MM; 80 x 12.5 MM; 80 x 15 MM Knee joint…

Biomet, Inc.

Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.

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: Biomet, Inc. · 56 E Bell Dr · Warsaw, IN · 46582-6989

Is this the product you have?

  • MCK Maximum Congruent Knee System, BIOMET FINNED PRI STEM 40MM; 80 x 10MM; 80 x 12.5 MM; 80 x 15 MM Knee joint replacement prostheses components include femoral, tibial, and patellar components.
Lot codes and dates
  • Part Numbers
    • 141314
    • 141316
    • 141318
    • 141320
    • Use-by 2025-03-13
  • Lot Numbers

    79 of 79 codes

    • 035650
    • 035690
    • 065500
    • 066850
    • 066900
    • 066910
    • 066930
    • 066940
    • 066950
    • 066960
    • 066970
    • 066990
    • 067010
    • 104580
    • 104590
    • 104600
    • 104620
    • 104630
    • 104640
    • 104650
    • 104660
    • 125820
    • 125830
    • 125840
    • 129180
    • 183220
    • 183230
    • 183240
    • 183250
    • 183260
    • 183270
    • 183280
    • 183290
    • 183300
    • 183310
    • 183320
    • 257770
    • 257780
    • 257790
    • 257810
    • 257850
    • 257860
    • 257870
    • 257880
    • 299730
    • 299750
    • 299760
    • 299780
    • 299800
    • 299810
    • 299820
    • 842220
    • 951620
    • 954160
    • 997470
    • 023580
    • 077970
    • 125850
    • 251680
    • 335490
Amount recalled
1315

This recall covers 5 products

The agency filed one notice per product. You are reading one of them; the other 4 are below.

Where it was sold

Why it was recalled

Biomet hip joint, knee joint and shoulder joint replacement components device labeling contains incorrect GTIN (Global Trade Identification Number) codes.

This product is unlikely to cause harm, but it breaks a safety or labelling rule.

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.

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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 16, 2016 · Data as of Sep 19, 5:30 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.