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Biomet, Inc. recalls Compress Face Reamer Product Usage: Correction of revision of unsuccessful osteotomy, arthrodesis, or previous joi
Recalled October 15, 2014 · FDA recall Z-0021-2015 · Biomet
Hazard
Investigation determined that units supplied were missing the 4x21 degree helix angle. · FDA Class II
Units
4
Sold at
International Distribution in the countries of Netherlands, Europe, the Middle East, and Asia.
Description
Investigation determined that units supplied were missing the 4x21 degree helix angle.
Product
Compress Face Reamer Product Usage: Correction of revision of unsuccessful osteotomy, arthrodesis, or previous joint replacement, tumor resections, revision of previously failed total joint arthroplasty, and trauma.
Manufacturer(s)
Biomet, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →