FDA DeviceClass IINotable

FDA Recall: Intramedullary Bone Saw Blade Assembly Model/Catalog Number: 475640 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

11

View original recall →
Share:

Related Recalls

2026-08-12 · FDA_DEVICE
FDA Recall: Intramedullary Bone Saw Blade Assembly Model/Catalog Number: 475630 Product Description: Intramedu
Biomet, Inc.
2026-08-12 · FDA_DEVICE
FDA Recall: Intramedullary Bone Saw Blade Assembly Model/Catalog Number: 475625 Product Description: Intramedu
Biomet, Inc.
2026-08-12 · FDA_DEVICE
FDA Recall: Intramedullary Bone Saw Blade Assembly Model/Catalog Number: 475620 Product Description: Intramedu
Biomet, Inc.
2026-08-12 · FDA_DEVICE
FDA Recall: Intramedullary Bone Saw Blade Assembly Model/Catalog Number: 475635 Product Description: Intramedu
Biomet, Inc.