Zimmer Biomet, Inc. recalls PERIARTICULAR PLATES - FEMUR, Item Nos. 00234700106 00234700108 00234700110 00234700112 00234700114 00234700116 0023470…
- Recall date
- October 10, 2019
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Recall number
- Z-0308-2020
- FDA classification
- Class II
- Brand / firm
- Zimmer Biomet, Inc.
- Sold / distributed
- Distributed nationwide.
Why it was recalled
Non-highly polished implants may adhere to the LDPE bag (previous packaging configuration).
Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.
What was recalled
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
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