Biomet, Inc.: Medical Device Recall in 2014 - (Recall #: Z-1244-2014)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2014.

Data Source: FDA.

Product Description:

Part 475630, Intramedullary Bone Saw, Cam Assembly Size 14 mm, The Biomet Intramedullary Bone Saw is a unique and exclusive clinical instrument that is used to correct leg length, or rotational discrepancies in the femur.

Product Classification:

Class II

Date Initiated: February 26, 2014

Date Posted: March 26, 2014

Recall Number: Z-1244-2014

Event ID: 67618

Reason for Recall:

Incorrect labeling on specific lots of the Intramedullary Bone Saw. The Saw Blade Assembly was identified as CAM Assembly.

Status: Terminated

Product Quantity: 6

Code Information:

Lot 239470, 457450

Distribution Pattern:

Worldwide Distribution: US (nationwide) to states of: NY, TX, MI, and M; to countries of: Australia and The Netherlands.

Voluntary or Mandated:

Voluntary: Firm initiated