Is Biomet, Inc. recalled?

Yes — a recall has been published. 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.

TemporaryFDAOngoing

Can cause harm that is usually temporary.

Intramedullary Bone Saw Blade Assembly Model/Catalog Number: 475630 Product Description: Intramedullary Bone Saw Blade Assembly 14mm

Check the device or its packaging for

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

Why: 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.
Distributed: 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.
Company: Biomet, Inc.
Announced: 12 August 2026This is the date the recall was announced. A company may have started it weeks earlier.
Recall began: 1 July 2026

Source: FDA record Z-2869-2026 · retrieved 3 August 2026

Read the official notice

Every recall is shown word for word from the FDA and USDA, with a link to the source.