CALCANAIL® 268323- CALCANAIL CANNULATED SCREW Ø5 LG36MMRecalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 03661489683237), received between Dec 22, 2022 and Dec 22, 2022 — classified as 1 malfunction.

The most frequently reported specific device problem is “Material Deformation” (1 report).

Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. What reports can and can't tell you · How this data works · Data updated Oct 18, 2026.

Most reported problems

Recent adverse event reports

The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

• MalfunctionDec 22, 2022Material Deformation; Material Deformation

  THREAD SEAL WHEN TIGHTENING THE CANULATED SCREW INTO THE CALCANEAL WAIL HOLE. COMPLAINT ON THE REFERENCE : (B)(4). - FDA EQUIVALENCE : (B)(4).

  Patient problems: Insufficient Information

  MAUDE report 16038742 ↗