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Zimmer Biomet, Inc. recalls PERIARTICULAR PLATES SHOULDER, PERI PROX LAT HUMERAL, Item Nos. 00234800104 00234800106 00234800108 00234800110 0023
Recalled November 13, 2019 · FDA recall Z-0313-2020 · 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 SHOULDER, PERI PROX LAT HUMERAL, Item Nos. 00234800104 00234800106 00234800108 00234800110 00234800112 00234800114 00234800116 00234800204 00234800206 00234800208 00234800210 00234800212 00234800214 00234800216 00234800304 00234800306 00234800404 00234800408 00234800412
Manufacturer(s)
Zimmer Biomet, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →