Official recall notice
FDA DeviceClass IINotable
FDA Recall: Intramedullary Bone Saw Blade Assembly Model/Catalog Number: 475630 Product Description: Intramedu
- Recall date
- 2026-08-12
- Brand
- Biomet, Inc.
- Category
- Medical Device
- FDA class
- Class II
Why it was recalled
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.
Product 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.
Affected products
UDI-DI (01)00887868507816(17)360221(10)67818764; Lot 67818764 Model No 475630; UDI-DI (01)00887868507816(17)360401(10)67818768; Lot 67818768 Model No 475630; UDI-DI (01)00887868507816(17)360428(10)67954534; Lot 67954534