FDA Medical devices recall ·
MICS3 Angled Sagittal Saw Attachment recall
- Recall number
- Z-1572-2026
- Date
- (initiated February 2, 2026)
- Company / brand
- Howmedica Osteonics Corp.
325 Corporate Dr, Mahwah, NJ, United States - Category
- Medical devices › Class II
- Classification
- Class II
- Status
- Ongoing
- Units affected
- 1098 units
- Initiated by
- Voluntary: Firm initiated
Read the official FDA notice ↗
Product
MICS3 Angled Sagittal Saw Attachment; Part Number: 210490
Why was it recalled?
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.
What should you do?
FDA enforcement reports do not list a consumer remedy. Check the product codes below against what you have; if it matches, stop using it and follow the instructions in the firm's or FDA's official notice, or contact the company. If you have health concerns, contact your healthcare provider.
Product codes & lot numbers
Part Number: 210490; UDI: (01)07613327523874(10)TU6563205RP; Lot numbers: ALL;
Distribution
Domestic: Nationwide Distribution; International: Australia, Germany, Belgium, France, Spain UK, New Zealand;
What does Class II mean?
Class II means use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or the probability of serious harm is remote.
Source: FDA (medical devices), recall Z-1572-2026. Official notice. Republished from public data; RecallFlag is not affiliated with the FDA.