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Zimmer Biomet, Inc. recalls FEMOROTIBIAL/FEMORAL NAIL, various sizes. Item Nos. 32855331111 32855331113 32855331115 32855331161 32855331163 328
Recalled November 13, 2019 · FDA recall Z-0333-2020 · Zimmer Biomet
Hazard
Non-highly polished implants may adhere to the LDPE bag (previous packaging configuration). · FDA Class II
Units
5,459,583 total devices
Sold at
Distributed nationwide.
Description
Non-highly polished implants may adhere to the LDPE bag (previous packaging configuration).
Product
FEMOROTIBIAL/FEMORAL NAIL, various sizes. Item Nos. 32855331111 32855331113 32855331115 32855331161 32855331163 32855331165
Manufacturer(s)
Zimmer Biomet, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →