FDA Enforcement Class II Terminated

Biomet Orthopedics Intramedullary Bone Saw Cam Assembly 13MM-Orthopedic manual surgical instrument Item Number: 475660

Recall: Z-0594-2020 · Reported December 11, 2019

Enforcement

Recall Number
Z-0594-2020
Event ID
84224
Classification
Class II
Status
Terminated
Product Type
Devices
Firm
Zimmer Biomet, Inc.
Voluntary / Mandated
Voluntary: Firm initiated
Initial Notification
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Report Date
December 11, 2019
Initiation Date
October 25, 2019
Classification Date
December 3, 2019
Termination Date
April 30, 2020
Address
56 E Bell Dr, Warsaw, IN, 46582-6989, United States

Description

Biomet Orthopedics Intramedullary Bone Saw Cam Assembly 13MM-Orthopedic manual surgical instrument Item Number: 475660

Reason

Possible commingle of 13 MM and 14 MM Intramedullary Bone Saw Cam Assembly -an Intramedullary Bone Saw Cam Assembly was labeled and etched as a 14 MM but measured as a 13 MM cam

Code Info

Lot Numbers: 025800, 025810, 081640 UDI: (01)00880304386570(17)280202(10)025800 (01)00880304386570(17)280205(10)025810 (01)00880304386570(17)280524(10)081640

Distribution

Distribution to US states of CA, FL, IN, MN, MO, NY, and UT, Australia, and New Zealand

Quantity

26 units