Portex 100/199/050Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 15019315022289), received between Mar 28, 2022 and Mar 28, 2022 — classified as 1 malfunction.

The most frequently reported specific device problem is “Inflation Problem” (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 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

• MalfunctionMar 28, 2022Inflation Problem; Inflation Problem

  IT WAS REPORTED THAT WHEN THE CUSTOMER PUT AIR IN THE CUFF DURING THE PRE-USE CHECK, MORE RESISTANCE THAN USUAL WAS FELT THROUGH THE PRODUCT. THERE WAS NO PATIENT INJURY REPORTED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 13930697 ↗