FDA recall, , Moderate risk
Howmedica Osteonics MICS3 Angled Sagittal Saw Attachment
The MICS3 Angled Sagittal Saw Attachment has screws that may loosen and detach during use.
Summary by Recall Canary from the FDA notice
What happened
Howmedica Osteonics Corp. of Mahwah, New Jersey, began a recall on February 2, 2026, of the MICS3 Angled Sagittal Saw Attachment because the external screws that secure the cover to the Angled Saw Housing may loosen during use and detach from the attachment. The recall was added to the FDA's Enforcement Report on March 18, 2026, and was classified by the FDA on the same date.
The product was distributed nationwide in the U.S. and internationally to Australia, Germany, Belgium, France, Spain, UK, and New Zealand. The recall affects 1098 units.
What to do
We don't have product-specific instructions for this recall. FDA's general advice for medical device recalls:
- A device recall doesn't always mean you must stop using it: it may need to be checked, adjusted or fixed.
- Talk to your health care provider before you stop using it.
Is yours affected?
Match the UDI-DI and part code listed under your product.
A UDI-DI is the device identifier printed with the barcode on the device label.
MICS3 Angled Sagittal Saw Attachment
- UDI-DI
- 07613327523874
- Part code
- 210490
Recall details
- Company began the recall
- Sold in
Domestic: Nationwide Distribution; International: Australia, Germany, Belgium, France, Spain UK, New Zealand;
- Company
- Howmedica Osteonics Corp.Mahwah, New Jersey
- Hazard
- Device defect
- Risk
Moderate risk
Using it may cause short-term health problems, or ones that treatment can reverse. Serious harm is unlikely.
FDA Class II recall · How risk is rated
- Event ID
- 98411
- Recall number
- Z-1572-2026
- Quantity recalled
- 1098 units
All recalls from Howmedica Osteonics Corp.
Timeline
FDA's Enforcement Report is its public list of recalls; FDA adds a recall when it posts it and publishes the list weekly.
Company began the recall
Added to FDA's Enforcement Report · Classified by FDA
In FDA's weekly enforcement report
Listed on Recall Canary
Summary updated
