Z-0304-2020 Class II Terminated

Recalled by Zimmer Biomet, Inc. — Warsaw, IN

Recall Details

Product Type
Devices
Report Date
November 13, 2019
Initiation Date
October 10, 2019
Termination Date
May 19, 2020
Voluntary/Mandated
Voluntary: Firm initiated
Product Quantity
5,459,583 total devices

Product Description

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 0202264121 0202265010 0202265012 0202265014

Reason for Recall

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

Distribution Pattern

Distributed nationwide.

Code Information

All product manufactured prior to January 2014.