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Zimmer Biomet, Inc. recalls PERIARTICULAR PLATES - FEMUR, Item Nos. 00234700106 00234700108 00234700110 00234700112 00234700114 00234700116 00
Recalled November 13, 2019 · FDA recall Z-0308-2020 · 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
PERIARTICULAR PLATES - FEMUR, Item Nos. 00234700106 00234700108 00234700110 00234700112 00234700114 00234700116 00234700118 00234700206 00234700208 00234700210 00234700212 00234700214 00234700216 00234700218 00234703104 00234703106 00234703108 00234703204 00234703206 00234703208
Manufacturer(s)
Zimmer Biomet, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →