FDA DeviceClass IINotable

FDA Recall: Intramedullary Bone Saw Blade Assembly Model/Catalog Number: 475635 Product Description: Intramedu

Date: 2026-08-12
Brand: Biomet, Inc.
Category: Medical Device
FDA Class: Class II

Description

Zimmer Biomet is conducting a medical device recall removal for various sizes of the Intramedullary Bone Saw Blade Assembly due to potential sterile barrier packaging damage caused by an exposed saw blade.

Hazard

Zimmer Biomet is conducting a medical device recall removal for various sizes of the Intramedullary Bone Saw Blade Assembly due to potential sterile barrier packaging damage caused by an exposed saw blade.

Remedy

22

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