Reported May 1, 2024 · Ongoing
TRIDENTII HEMI CLUSTER66H- Indicated for use in primary and revision patients at high risk of hip dislocation Catalog…
Howmedica Osteonics Corp.
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: Howmedica Osteonics Corp. · 325 Corporate Dr · Mahwah, NJ · 07430-2006
Is this the product you have?
- TRIDENTII HEMI CLUSTER66H- Indicated for use in primary and revision patients at high
- risk of hip dislocation Catalog Number702-11-66H
- Lot codes and dates
- UDI-DI(01)07613327380835(17)290313(10)
- Lot Number15445252
- Amount recalled
- 0
This recall covers 12 products
The agency filed one notice per product. You are reading one of them; the other 11 are below.
Where it was sold
- Nationwide
Why it was recalled
The acetabular shell may have excessive deburring, resulting in a smooth surface on the edge of the shell
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.
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