Reported Jun 17, 2015 · Terminated
Biomet Cobalt-Chrome Femoral Components, 32MM MOD HEAD COCR -6MM NECK; 32MM MOD HEAD COCR -3 MM NECK; 32MM MOD HEAD…
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?
Biomet Cobalt-Chrome Femoral Components32MM MOD HEAD COCR -6MM NECK32MM MOD HEAD COCR -3 MM NECK32MM MOD HEAD COCR STD NECK32MM MOD HEAD COCR +3MM NECK32MM COCR MOD HD +6MM NO SKIRT Hip
- joint replacement components includefemoral stems, femoral heads, acetabular shells, and acetabular liners
- Lot codes and dates
- Part Numbers
163667163668163669163670163674Use-by 2025-03-18
- Lot Numbers
331620331650453080453090453110453120489140453180471380471410044600332720375590375620375630375640375650465840466050470060471430471440471450375660375670375700453220
- Part Numbers
- 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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