Dover 68800Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10884521008236), received between Dec 19, 2019 and Dec 19, 2019 — classified as 1 malfunction.

The most frequently reported specific device problem is “Decrease in Suction” (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. How this data works · Data updated Oct 13, 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.

• MalfunctionDec 19, 2019Decrease in Suction; Decrease in Suction

  THE CUSTOMER REPORTED THAT THE LARGE 60CC SYRINGE DOES CREATE ENOUGH SUCTION TO PULL OUT AND MEASURE THE STOMACH CONTENTS OF PATIENTS. IT GIVES A FALSE SENSE THAT THERE IS NO RESIDUAL, WHEN ACTUALLY THE PATIENT HAS A LARGE RESIDUAL. A PATIENT WAS OVERFED AND ASPIRATED DURING THE TIME RESIDUALS WERE MARKED AS ZERO. IT WAS SUSPECTED BY THE CUSTOMER BUT NOT CONFIRMED THAT IT WAS RELATED TO HIGH RESIDUALS AND CONTINUED FEEDING OF THE PATIENT. THE PATIENT INVOLVED HAD MULTIPLE CO-MORBIDITIES AND WAS EVENTUALLY TERMINALLY EXTUBATED AND GIVEN COMFORT CARE. THE CUSTOMER STATED THE FAMILY¿S DECISION WAS NOT RELATED TO THE ASPIRATION.

  Patient problems: Aspiration/Inhalation

  MAUDE report 9494803 ↗