medical Class II Updated 2019-11-13

Zimmer Biomet, Inc. recalls PERIARTICULAR PLATES - FEMUR, Item Nos. 00234700106 0023470

Recalled 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

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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