FDA Enforcement Class II Terminated

Part 475620 Intramedullary Bone Saw CAM Assembly Size 12mm, A unique and exclusive clinical instrument used to correct leg length, or rotational discrepancies in the femur.

Recall: Z-1242-2014 · Reported March 26, 2014

Enforcement

Recall Number
Z-1242-2014
Event ID
67618
Classification
Class II
Status
Terminated
Product Type
Devices
Firm
Biomet, Inc.
Voluntary / Mandated
Voluntary: Firm initiated
Initial Notification
E-Mail
Report Date
March 26, 2014
Initiation Date
February 26, 2014
Classification Date
March 20, 2014
Termination Date
July 7, 2015
Address
56 E Bell Dr, Warsaw, IN, 46582-6989, United States

Description

Part 475620 Intramedullary Bone Saw CAM Assembly Size 12mm, A unique and exclusive clinical instrument used to correct leg length, or rotational discrepancies in the femur.

Reason

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

Code Info

Lot 669420

Distribution

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

Quantity

1