CLASS II ONGOING Device recall · Reported 25 Mar 2026 · FDA Enforcement Report

MICS3 Angled Sagittal Saw Attachment recalled by Howmedica Osteonics

Howmedica Osteonics is recalling MICS3 Angled Sagittal Saw Attachment, distributed nationwide in the US. The recall was initiated on 2 Feb 2026 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesPart Number: 210490; UDI: (01)07613327523874(10)TU6563205RP; Lot numbers: ALL;

Quantity recalled1098 units

Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.

Recall details

Recall number: Z-1572-2026
FDA event ID: 98411
Recalling firm: Howmedica Osteonics, Mahwah, NJ
Classification: Class II
Status: Ongoing
Recall initiated: 2 Feb 2026
FDA classified: 18 Mar 2026
Reported: 25 Mar 2026
Type: Voluntary: Firm initiated
Customers notified by: Letter
Reason category: Other Reasons
Device type: Other Medical Devices

Timeline

2 Feb 2026	Recall initiated by company
18 Mar 2026	Classified by FDA	+44 days
25 Mar 2026	Published in enforcement report	+7 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

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.

Product as listed by the FDA

MICS3 Angled Sagittal Saw Attachment; Part Number: 210490

Where it was distributed

Domestic: Nationwide Distribution; International: Australia, Germany, Belgium, France, Spain UK, New Zealand;

Nationwide

Questions about this recall

Why was it recalled?

Which lots are affected?

Part Number: 210490; UDI: (01)07613327523874(10)TU6563205RP; Lot numbers: ALL;

Where was it sold?

Domestic: Nationwide Distribution; International: Australia, Germany, Belgium, France, Spain UK, New Zealand;

What should I do if I have it?

Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.

What does Class II mean?

Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.

Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

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