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FDA · Medical devices ·

Intramedullary Bone Saw Blade Assembly Model/Catalog Number recall

Biomet, Inc. recalled Intramedullary Bone Saw Blade Assembly Model/Catalog Number on August 12, 2026 because of 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. It was sold in Refer to the attached ZFA 2026-00096_Initial Consignee List and ZFA 2026-00096_Initial Di….

Why it was recalled

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.

What's recalled

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

Quantity: 26

What to do

Check whether you have the product (match the lot numbers, dates or codes in the official notice). Stop using it, and return it or throw it away as the notice says.

Read the official FDA notice

Details

Company
Biomet, Inc., Warsaw, IN
Date
Severity
Class II
the product could cause temporary or reversible health problems.
Where sold
Refer to the attached ZFA 2026-00096_Initial Consignee List and ZFA 2026-00096_Initial Di…
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.
Status
Ongoing
Recall number
Z-2869-2026
Source
U.S. Food and Drug Administration

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