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Recall Observatory FDA recall evidence

Device product

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.

Z-1244-2014

February 26, 2014

Class II

Product summary

Firm
Biomet, Inc.
Event
Event 67618
Status
Terminated
Classification
Class II
Quantity
6
Official record key
device-enforcement:Z-1244-2014

Official wording

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

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.

Derived failure modes

  • Labeling or packaging

    reason.labeling_packaging · v1.0.0

    Incorrect labeling