INTUITION 2525-30-400Recalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 10603295544579), received between May 5, 2025 and Jul 22, 2025 — classified as 2 malfunctions.

The most frequently reported specific device problem is “Incorrect Measurement” (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 16, 2026.

Most reported problems

Recent adverse event reports

The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.

• MalfunctionJul 22, 2025Material Deformation; Material Deformation

  IT WAS REPORTED THAT INTRAOPERATIVELY DURING A SURGERY WITH A SHORT-TERM-LOANER KIT THE SURGEON FOUND THE ATT CUTTING BLOCK LM4 TO BE WARPED. THIS CAUSED A SURGERY PROLONGATION OF ABOUT 10 MINUTES.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 22565859 ↗
• MalfunctionMay 5, 2025Incorrect Measurement; No Apparent Adverse Event; Incorrect Measurement; No Apparent Adverse Event

  IT WAS REPORTED THAT ON (B)(6) 2025, THE PERSON IN CHARGE CHECKED THE PRODUCTS AND FOUND THAT THERE WERE DIFFERENCES BETWEEN THE PRODUCTS AND THE CAD MODELS. SPECIFICALLY, THE DIFFERENCES ARE AS FOLLOWS: CHISEL ACTUALLY GOES APPROXIMATELY 1MM DEEPER THAN IT¿S OBSERVED IN NX MODELS FOR ALL FINISHING GUIDES LM SZ 1-4 ON MY END. SIZE 2 LM SHOWN BELOW. NO SURGICAL DELAY. NO PATIENT CONSEQUENCES.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 21963698 ↗