Zimmer Biomet, Inc.: Medical Device Recall in 2019 - (Recall #: Z-0594-2020)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2019.

Data Source: FDA.

Product Description:

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

Product Classification:

Class II

Date Initiated: October 25, 2019

Date Posted: December 11, 2019

Recall Number: Z-0594-2020

Event ID: 84224

Reason for Recall:

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

Status: Terminated

Product Quantity: 26 units

Code Information:

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 Pattern:

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

Voluntary or Mandated:

Voluntary: Firm initiated