FDAHealthJuly 1, 2026
Biomet, Inc. — Intramedullary Bone Saw Blade Assembly Model/Catalog Number: 475640 Product Description: Intramedullary Bone Saw Blade Assembly 16mm
⚠️ 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.
Is this relevant to me?
- Geography
- Unknown
- Source agency
- FDA
- Category
- Health
- Published
- July 1, 2026
Refer to the attached ZFA 2026-00096_Initial Consignee List and ZFA 2026-00096_Initial Distribution History containing the distribution and the identification of the affected consignees.
What's affected?
- Product
- Intramedullary Bone Saw Blade Assembly Model/Catalog Number: 475640 Product Description: Intramedullary Bone Saw Blade Assembly 16mm
- Brand
- Biomet, Inc.
- Lot code
- 67818792
Additional details
UDI-DI (01)00887868507830(17)360316(10)67818792; Lot 67818792
What should I do?
Recommended action
Class II recall. Voluntary: Firm initiated Quantity affected: 11.
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