medical Class II Updated 2019-11-13

Zimmer Biomet, Inc. recalls PERIARTICULAR PLATES SHOULDER, PERI PROX LAT HUMERAL, Item N

Recalled 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

Hazard / Issue

Non-highly polished implants may adhere to the LDPE bag (previous packaging configuration).

Issued by

FDA

Distribution: Nationwide (United States)
Lot/Code Info: All product manufactured prior to January 2014.
View official government recall

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