NA 4810-30-540Recalls & reported problems

Summary

The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 10603295509783), received between Apr 30, 2025 and Jun 10, 2025 — classified as 3 malfunctions.

The most frequently reported specific device problem is “Material Deformation” (3 reports).

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. How this data works · Data updated Oct 13, 2026.

Most reported problems

Recent adverse event reports

The 3 most recent of 3 reports, in the reporter's own words as published by the FDA.

• MalfunctionJun 10, 2025Material Deformation; Material Deformation

  IT WAS REPORTED THAT THE DEPTH GAUGE IS BENT. NO PATIENT WAS HARMED OR AFFECTED. THE EVENT DID NOT HAPPEN IN SURGERY.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 22174711 ↗
• MalfunctionApr 30, 2025Material Deformation; Material Deformation

  IT WAS REPORTED THAT TWO DEPTH GAUGES WERE BENT/MANGLED AND NEEDED TO BE REPLACED. NO PATIENT WAS HARMED OR AFFECTED. THE EVENT DID NOT HAPPEN IN SURGERY.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 21936625 ↗
• MalfunctionApr 30, 2025Material Deformation; Material Deformation

  IT WAS REPORTED THAT TWO DEPTH GAUGES WERE BENT/MANGLED AND NEEDED TO BE REPLACED. NO PATIENT WAS HARMED OR AFFECTED. THE EVENT DID NOT HAPPEN IN SURGERY.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 21936623 ↗