Biomet recalls Intramedullary Bone Saw Blade Assembly Model 475640 due to potential sterile packaging damage from exposed saw blades. Affected medical devices may pose infection risks during surgery.
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.
Biomet is recalling a specific bone saw blade assembly model because it might damage the sterile packaging, which could lead to infections during surgery. This is a medical device recall for surgeons and hospitals using this product.
The saw blade assembly might cause damage to the sterile packaging during use, which could lead to contamination or infection if the blade is exposed. This is a medical device that requires strict sterile conditions during surgical procedures.
Surgeons and hospitals that use the Intramedullary Bone Saw Blade Assembly Model 475640 are most at risk. The recall affects medical devices used in orthopedic surgeries.
Check for the model number 475640 on the packaging or device. The product was sold with specific lot numbers including 67818792. This recall applies to medical devices used in orthopedic surgeries.
Look for the model number 475640 and lot number 67818792 on the packaging or device.
Biomet recalls this bone saw blade assembly due to potential damage to sterile packaging from an exposed saw blade, which could lead to infection risks during surgery.
Check for model number 475640 and lot number 67818792 on the packaging or device.
The recall does not specify a remedy, so contact Biomet directly for guidance on next steps.
We’ve drafted a message you can send Biomet to request your refund or repair — edit it as you like.
Subject: Recall Z-2871-2026 — Biomet Biomet Hello, I own a Biomet that is covered by recall Z-2871-2026 from Biomet. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
