SPECIALIST 96-6318Recalls & reported problems

Summary

The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 10603295247821), received between Jan 30, 2019 and Jan 30, 2019 — 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. 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 3 most recent of 3 reports, in the reporter's own words as published by the FDA.

• MalfunctionJan 30, 2019Material Deformation; Mechanical Jam; Material Deformation; Mechanical Jam

  IT WAS REPORTED THAT THE SURGEON FEELS LIKE HIS SAW BLADE WAS GETTING STUCK IN THE GUIDES.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 8289540 ↗
• MalfunctionJan 30, 2019Material Deformation; Mechanical Jam; Material Deformation; Mechanical Jam

  IT WAS REPORTED THAT THE SURGEON FEELS LIKE HIS SAW BLADE WAS GETTING STUCK IN THE GUIDES.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 8289531 ↗
• MalfunctionJan 30, 2019Material Deformation; Mechanical Jam; Material Deformation; Mechanical Jam

  IT WAS REPORTED THAT THE SURGEON FEELS LIKE HIS SAW BLADE WAS GETTING STUCK IN THE GUIDES.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 8289518 ↗