Vital Signs 5102RVWRecalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10885403272134), received between Nov 10, 2021 and Nov 10, 2021 — classified as 1 injury.

The most frequently reported specific device problem is “Mechanical 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 18, 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.

• InjuryNov 10, 2021Mechanical Problem; Mechanical Problem

  THE CUSTOMER REPORTED THAT THE VITAL SIGNS¿ FLOW INFLATING TAIL-END VALVE TRANSPORT CIRCUIT, FLOW-INFLATING TRA EXPERIENCED VALVE CLOSES TOO EASILY WHICH CAUSED HIGH PRESSURES TO ENTER LUNGS AND RESULTED IN PNEUMOTHORAX. AS AN INTERVENTION, INTUBATED INFANT BEING GIVEN MANUAL BREATHS.

  Patient problems: Pneumothorax

  MAUDE report 12788935 ↗