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Howmedica Osteonics Corp. recalls 28MM -4 LFIT V40 HEAD, Catalog Number 6260-9-122
Recalled December 8, 2021 · FDA recall Z-0314-2022 · Howmedica Osteonics
Hazard
There is a potential for the outer white Tyvek lid to debond from the sealed package. · FDA Class II
Sold at
Puerto Rico
Description
There is a potential for the outer white Tyvek lid to debond from the sealed package.
Product
28MM -4 LFIT V40 HEAD, Catalog Number 6260-9-122
Manufacturer(s)
Howmedica Osteonics Corp.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →