OTHER DYNJINFL8DRecalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 10197344110797), received between May 6, 2025 and May 6, 2025 — classified as 2 injuries.

The most frequently reported specific device problem is “Inflation Problem” (2 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 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.

• InjuryMay 6, 2025Inflation Problem; Inflation Problem

  RAPID JUMP OF ATMOSPHERES OF THE DIGITAL INFLATION DEVICE.

  Patient problems: Perforation

  MAUDE report 21970622 ↗
• InjuryMay 6, 2025Inflation Problem; Inflation Problem

  RAPID JUMP OF ATMOSPHERES OF THE DIGITAL INFLATION DEVICE.

  Patient problems: Perforation

  MAUDE report 21969973 ↗