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