Recall Z-2867-2026— Biomet, Inc.
Class II · Ongoing
Class II FDA medical device recall by Biomet, Inc., initiated 2026-07-01. FDA's recall record names no specific 510(k) clearance for this event. Product: Intramedullary Bone Saw Blade Assembly Model/Catalog Number: 475620 Product Description: Intramedullary Bone Saw Blade Assembly 12mm. Reason: 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..
- Recalling firm
- Biomet, Inc.
- Classification
- Class II
- Status
- Ongoing
- Initiated
- 2026-07-01
- Firm location
- Warsaw, IN, United States
Product description
Intramedullary Bone Saw Blade Assembly Model/Catalog Number: 475620 Product Description: Intramedullary Bone Saw Blade Assembly 12mm
Reason for recall
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.
Data sourced from openFDA. This site is unofficial and independent of the FDA.