# FDA device recall: Intramedullary Bone Saw Blade Assembly  Model/Catalog Number: 475640  Product Description: Intramedullary Bone Saw Blade

> recall · VERIFIED · 2026-07-01

Firm: Biomet, Inc. · Class II · 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 b

- Company: Biomet, Inc.
- Sector: medical devices
- Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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Source: MedFuel Intel news monitor. Verification tier: VERIFIED. Informational only, not investment advice. Corrections: media@medfuelinc.com.