Howmedica Osteonics recalls MICS3 Angled Sagittal Saw Attachment (Part 210490) due to potential screw loosening during use that could cause detachment. All units are affected.
A potential issue was identified with the torque strength on the external screws of the MICS3 Angled Sagittal Saw Attachment. These screws, which secure the cover to the Angled Saw Housing, may loosen during use and detach from the attachment.
Howmedica Osteonics is recalling its MICS3 Angled Sagittal Saw Attachment (Part Number 210490) because screws may loosen and detach during use. This could lead to the attachment becoming unstable or causing injury during surgical procedures.
The external screws that secure the attachment cover to the saw housing may loosen during use. If the screws detach, the attachment could become unstable or cause injury during surgical procedures.
Surgical professionals using the MICS3 Angled Sagittal Saw Attachment for medical procedures are most at risk. All units produced are affected.
Check for the Part Number 210490 on the attachment. All units are affected regardless of lot number or date of sale.
Inspect the screws securing the cover to the saw housing for looseness or signs of detachment.
Reach out to Howmedica Osteonics for guidance on fixing the issue if screws are loose.
Yes, all units of the MICS3 Angled Sagittal Saw Attachment with Part Number 210490 are affected.
Check if the screws securing the cover to the saw housing are loose or have detached.
Contact Howmedica Osteonics for guidance on repairing the issue.
We’ve drafted a message you can send Howmedica Osteonics to request your refund or repair — edit it as you like.
Subject: Recall Z-1572-2026 — Howmedica Osteonics Howmedica Osteonics Hello, I own a Howmedica Osteonics that is covered by recall Z-1572-2026 from Howmedica Osteonics. 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.