Product Wiki · Recalls · U.S. FDA — Device Enforcement

Recall Z-0304-2020 — NCB PERIPROSTHETIC, "NCB PP PROX FEM PLATE", Various sizes, Item Nos. 0202263009 0202263012 0202263015 0202263018 0202263021 0202263109 0202263112 0202263115 0202263118 0202263121 0202264009 0202264012 0202264015 0202264018 0202264021 0202264109 0202264112 0202264115 0202264118 02

U.S. FDA — Device Enforcement · United States · 2019-10-10 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-0304-2020
Date of alert
2019-10-10
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Zimmer Biomet, Inc.
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
0202263009
Reported risk: Non-highly polished implants may adhere to the LDPE bag (previous packaging configuration).
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

Verify each fact at the issuing agency before acting. Recall scope, affected lots, and remediation instructions may be updated by the agency after our last sync.

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