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Zimmer Biomet, Inc. recalls LPS-MOB ART SURF IMPL D 9MM
Recalled November 13, 2019 · FDA recall Z-0324-2020 · 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
LPS-MOB ART SURF IMPL D 9MM
Manufacturer(s)
Zimmer Biomet, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →