FDAFDA · Food and drugs·Recall number Z-1243-2014
Part 475625, Intramedullary Bone Saw, Cam Assembly Size 13 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.
Published March 26, 2014 · Recall initiated: February 26, 2014
Status when published: Terminated — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
Incorrect labeling on specific lots of the Intramedullary Bone Saw. The Saw Blade Assembly was identified as CAM Assembly.
What to do
Voluntary: Firm initiated · E-Mail
Recall details
- Manufacturer
- Biomet, Inc.
- Distributor
- Worldwide Distribution: US (nationwide) to states of: NY, TX, MI, and M; to countries of: Australia and The Netherlands.
- Lot
- Lot 239430, 239450
- Risk classification
- Class II
- Area (FDA)
- device
- Country
- United States
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