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Recall

MICS3 Angled Sagittal Saw Attachment; Part Number: 210490

Howmedica Osteonics Corp. · 2 Feb 2026

Status
Recall open, classified
Why, in the FDA's words
“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.”
Recall began
2 Feb 2026
Company
Howmedica Osteonics Corp.
Device type
Orthopedic stereotaxic instruments (knee, hip and spine robots) (OLO)
Concerns
K220459, K241011

What it means

A recall is the FDA's record that a company is correcting or removing a device because of a problem. Many are fixed with a software update or new instructions; the record does not say whether anyone was hurt. See our plain guide to FDA terms.

The record

The FDA publishes this record in its public device database. The summary documents the company filed, when available, are linked from the FDA's page.
FDA database