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Intramedullary bone saw blade assembly
Official notice
3 Jul 2026
Last checked
3 Jul 2026
An official Health Canada notice concerns Intramedullary bone saw blade assembly. Zimmer Biomet is conducting a medical device recall removal for various sizes of the Intramedullary Bone Sawblade Assembly due to potential sterile barrier packaging damaged caused by the exposed saw blade. It was identified internally that the tip protector was incorrectly placed on the blunt end of the device instead of the sawblade, leaving the saw blade exposed. The exposed saw blade has potential to damage the sterile barrier pouch, which has potential to result in loss of sterility. There have been zero complaints received. Published 2026-07-03.
What to do now
Contact the manufacturer if you require additional information.
Recall number
82280
Official notice
2026-07-03
The hazard
The hazard
Zimmer Biomet is conducting a medical device recall removal for various sizes of the Intramedullary Bone Sawblade Assembly due to potential sterile barrier packaging damaged caused by the exposed saw blade. It was identified internally that the tip protector was incorrectly placed on the blunt end of the device instead of the sawblade, leaving the saw blade exposed. The exposed saw blade has potential to damage the sterile barrier pouch, which has potential to result in loss of sterility. There have been zero complaints received.
How to check if you're affected
How to check if you're affected
Compare the VIN on your vehicle against the official list. If your VIN is listed, follow the official notice.
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The source does not list specific retailers. See the official notice for where affected vehicles were sold.
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Brand: Biomet Orthopedics Ata Biomet Sports Medicine Ata Biomet Biologics Ata Biomet Trauma.
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See the official notice and source documents for full details.
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