← FDA ENFORCEMENT
Z-1572-2026Class II

Howmedica Osteonics Corp.

What this record is not

A recall record is reproduced as FDA published it, and the classification is FDA’s. SPEQ adds no interpretation, and a recall concerns the products and dates in the record — it is not a statement about a company’s other products or its current status.

Recalling firm
Howmedica Osteonics Corp.
Product type
Device
Status
Ongoing
Report date
2026-03-25
Distribution
Domestic: Nationwide Distribution; International: Australia, Germany, Belgium, France, Spain UK, New Zealand;
Firm state
NJ
Product quantity
1098 units
Initiated by
Voluntary: Firm initiated
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 description

MICS3 Angled Sagittal Saw Attachment; Part Number: 210490

Code / lot info

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

Data: U.S. FDA. Recall details are as reported by the FDA. The quality-domain mapping and severity are a SPEQ editorial interpretation of the recall reason, not an official FDA classification. Open the enforcement explorer →