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Biomet, Inc. recalls Biomet Integral Centralizer Hip System, Lateralized Femoral Stem (Co-Cr-Mo), 9mm, 11mm, 13mm, 15mm, and 17mm
Recalled January 20, 2016 · FDA recall Z-0650-2016 · Biomet
Hazard
PMMA is listed as a material on the label but the product does not contain PMMA. · FDA Class II
Units
21
Sold at
Worldwide distribution. US nationwide including IA, UT, MN, PA, MO, OK, IL, OH, and WA; CANADA, and NETHERLANDS
Description
PMMA is listed as a material on the label but the product does not contain PMMA.
Product
Biomet Integral Centralizer Hip System, Lateralized Femoral Stem (Co-Cr-Mo), 9mm, 11mm, 13mm, 15mm, and 17mm
Manufacturer(s)
Biomet, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →