Public recall detail

Intramedullary Bone Saw Blade Assembly

2026-07-03

medium
Health products Health product recall
Quick summary

Quick summary: Intramedullary Bone Saw Blade Assembly. Reason: Health product recall. Category: Health products. Date: 2026-07-03.

Recommended action

Recommended action: compare your product with the official notice and follow the instructions published by the official source.

Recall details

Quick summary: Intramedullary Bone Saw Blade Assembly. Reason: Health product recall. Category: Health products. Date: 2026-07-03.

Official details

Affected product details

Structured information extracted from the official recall notice. Confirm the identifiers and instructions in the original notice.

BrandBiomet Orthopedics, Ata Biomet Sports Medicine, Ata Biomet Biologics, Ata Biomet Trauma
ProductIntramedullary Bone Saw Blade Assembly
IssueMedical devices - Sterility
Recall classType II
IdentificationRA-82280

Affected products

ProductIntramedullary Bone Saw Blade Assembly
Lot67818764
Model475630
Serial number67818764
DescriptionIntramedullary Bone Saw Blade Assembly
ProductIntramedullary Bone Saw Blade Assembly
Lot67818770
Model475635
Serial number67818770
DescriptionIntramedullary Bone Saw Blade Assembly
ProductIntramedullary Bone Saw Blade Assembly
Lot67818791
Model475620
Serial number67818791
DescriptionIntramedullary Bone Saw Blade Assembly

Issue

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.

What you should do

  • Contact the manufacturer if you require additional information.
Additional official information
AudienceHealthcare
CategoryHealth products - Medical devices - Orthopaedics
CompaniesBiomet Orthopedics, Ata Biomet Sports Medicine, Ata Biomet Biologics, Ata Biomet Trauma56 East Bell Drive, Warsaw, Indiana, United States, 46581
Recall date2026-06-24
Published byHealth Canada
Recall classType II
Alert / recall typeHealth product recall
Identification numberRA-82280
Background{}
CompaniesBiomet Orthopedics, Ata Biomet Sports Medicine, Ata Biomet Biologics, Ata Biomet Trauma56 East Bell Drive, Warsaw, Indiana, United States, 46581
AudiencesHealthcare
Source updated2026-07-03

Contains information licensed under the Open Government Licence – Canada. SafetyPulse is independent of the Government of Canada.

Official source Monitor products Back to recalls

Starting...

Related recalls

Similar recalls and safety notices.

Loading related recalls...