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.
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. Distribution: 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. Quantity: 10 Lot/code info: UDI-DI (01)00887868507793(17)360407(10)67818791; Lot 67818791
00887868507793
Official record: FDA (Device enforcement) ↗
Republished from the official source above; details can change — the source record controls.