Puritan Bennett G-760110DIUU-JPRecalls & reported problems

Summary

The FDA's MAUDE database contains 19 adverse event reports that list this exact device (DI 10884521180918), received between Jul 3, 2018 and Aug 3, 2021 — classified as 19 malfunctions.

The most frequently reported specific device problem is “No Flow” (17 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 19 most recent of 19 reports, in the reporter's own words as published by the FDA.

• MalfunctionAug 3, 2021No Flow; No Flow

  IT WAS REPORTED THAT WHILE IN USE ON A PATIENT, THE 760 VENTILATOR GENERATED AN ALARM, STOPPED WORKING, FAILED TO DELIVER BREATHS AND THE SAFETY VALVE OPENED. THE PATIENT WAS REMOVED FROM THE VENTILATOR AND WAS PLACED ON AN ALTERNATE VENTILATOR WITHOUT INJURY. ADDITIONALLY, WHEN THE POWER WAS TURNED ON AGAIN THE DEVICE DISPLAYED THE MESSAGE "POWER ON SELF-TEST (POST) FAILED".

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 12268893 ↗
• MalfunctionMay 24, 2021No Flow; Output Problem; No Flow; Output Problem

  IT WAS REPORTED THAT WHILE IN USE ON A PATIENT, THIS 760 VENTILATOR GENERATED A SAFETY VALVE OPEN ALARM AND VENTILATION STOPPED. THE PATIENT WAS REMOVED FROM THE VENTILATOR AND PLACED ON AN ALTERNATE VENTILATOR WITHOUT HARM.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 11872534 ↗
• MalfunctionJan 13, 2021No Flow; No Flow

  IT WAS REPORTED THAT DURING MAINTENANCE, THE 760 VENTILATOR FAILED THE POWER ON SELF TEST (POST). THE VENTILATOR WAS NOT IN USE ON A PATIENT AT THE TIME OF THE REPORTED EVENT.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 11167226 ↗
• MalfunctionJan 7, 2021Infusion or Flow Problem; No Flow; Infusion or Flow Problem; No Flow

  IT WAS REPORTED THAT DURING MAINTENANCE, THE 760 VENTILATOR GENERATED AN OXYGEN(O2) SUPPLY LOW PRESSURE ALARM EVEN THOUGH THE O2 PIPE WAS CONNECTED. THE VENTILATOR WAS NOT IN USE ON A PATIENT AT THE TIME OF THE REPORTED EVENT.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 11136152 ↗
• MalfunctionJul 10, 2020No Flow; No Flow

  IT WAS REPORTED THAT WHILE IN USE ON A PATIENT, THE 760 VENTILATOR GENERATED AN ALARM AND THE SAFETY VALVE OPENING INDICATOR WAS FOUND TO BE ILLUMINATED. IT WAS REPORTED THAT THE VENTILATION STOPPED. THE PATIENT WAS PLACED ON AN ALTERNATE VENTILATOR AND WAS NOT HARM AS RESULT OF THE EVENT.

  Patient problems: No Clinical Signs, Symptoms or Conditions; No Consequences Or Impact To Patient

  MAUDE report 10260962 ↗
• MalfunctionJun 29, 2020No Flow; No Flow

  IT WAS REPORTED THAT DURING USE ON A PATIENT, A 760 VENTILATOR GENERATED AN ALARM AND DISPLAYED POST (POWER ON SELF TEST) FAILURE. MANUAL VENTILATION HAD TO BE PERFORMED DUE TO LOSS OF VENTILATION AND THE PATIENT WAS TRANSFERRED TO AN ALTERNATE VENTILATOR WITHOUT ANY HARM.

  Patient problems: No Clinical Signs, Symptoms or Conditions; No Consequences Or Impact To Patient

  MAUDE report 10206720 ↗
• MalfunctionMar 17, 2020No Flow; Output Problem; No Flow; Output Problem

  IT WAS REPORTED THAT DURING SERVICING, A 760 VENTILATOR FAILED ITS POWER ON SELF TEST (POST). THE VENTILATOR WAS NOT IN USE ON A PATIENT AT THE TIME OF THE REPORTED EVENT.

  Patient problems: No Patient Involvement

  MAUDE report 9845686 ↗
• MalfunctionOct 31, 2019No Flow; No Flow

  IT WAS REPORTED THAT, WHILE IN USE ON A PATIENT, A 760 VENTILATOR GENERATED AN ALARM AND THE SAFETY VALVE OPENED, WHICH STOPPED VENT ILLATION. THE PATIENT WAS REMOVED FROM THE VENTILATOR AND PLACED ON AN ALTERNATE VENTILATOR WITH NO HARM OR INJURY.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 9260605 ↗
• MalfunctionOct 25, 2019No Flow; No Flow

  IT WAS REPORTED WHILE IN USE THIS 760 VENTILATOR ALARMED AND VENTILATION STOPPED. THE PATIENT WAS REMOVED FROM THE VENTILATOR AND PLACED ON AN ALTERNATE VENTILATOR WITH NO HARM REPORTED.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 9241554 ↗
• MalfunctionSep 23, 2019No Flow; No Flow

  IT WAS REPORTED THAT DURING USE ON A PATIENT, A 760 VENTILATOR STOPPED VENTILATION AND SAFETY VALVE WENT OPEN WITH AN ALARM. PATIENT WAS REMOVED FROM THE VENTILATOR AND PLACED ON AN ALTERNATE VENTILATOR WITH NO HARM REPORTED.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 9106451 ↗
• MalfunctionAug 19, 2019No Flow; No Flow

  IT WAS REPORTED THAT DURING USE ON A PATIENT, THE SAFETY VALVE OPENED AND VENTILATION STOPPED. THE PATIENT WAS TRANSFERRED TO AN ALTERNATE VENTILATOR WITH NO PATIENT HARM.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 8908051 ↗
• MalfunctionFeb 11, 2019No Flow; No Flow

  IT WAS REPORTED DURING USE ON A PATIENT, THE 760-VENTILATOR GENERATED A LOW OXYGEN SUPPLY PRESSURE ALARM APPROXIMATELY FIFTEEN MINUTES AFTER THE CANNULA WAS CHANGED. ADDITIONALLY, THE POWER ON SELF-TEST FAILED, SAFETY VALVE OPENED, AND VENTILATION STOPPED. MANUAL VENTILATION WAS IMMEDIATELY PERFORMED AND THE PATIENT WAS THEN TRANSFERRED TO AN ALTERNATE VENTILATOR WITHOUT HARM OR INJURY.

  Patient problems: No Code Available; No Consequences Or Impact To Patient

  MAUDE report 8324981 ↗
• MalfunctionNov 6, 2018Defective Alarm; Defective Alarm

  IT WAS REPORTED THAT THE 700 SERIES VENTILATOR FAILED POST (POWER ON SELF TEST) WITH AN ERROR MESSAGE. THE VENTILATOR WAS NOT IN USE ON A PATIENT AT THE TIME OF THE REPORTED EVENT.

  Patient problems: No Patient Involvement

  MAUDE report 8044522 ↗
• MalfunctionOct 22, 2018No Flow; No Flow

  IT WAS REPORTED THAT DURING USE ON A PATIENT, THE 740 VENTILATOR GENERATED AN ALARM AND VENTILATION STOPPED. THE PATIENT WAS TRANSFERRED TO AN ALTERNATE VENTILATOR WITH NO PATIENT HARM.

  Patient problems: No Code Available; No Consequences Or Impact To Patient

  MAUDE report 7992856 ↗
• MalfunctionSep 27, 2018No Flow; No Flow

  IT WAS REPORTED THAT DURING USE ON PATIENT THE 760 VENTILATOR HAD GENERATED VENTILATION FAILURE ALARM. THE DEVICE TURNED ON AGAIN THEN POST(POWER ON SELF TEST) FAILURE OCCURRED WITH ERROR CODES. THE PATIENT WAS REMOVED FROM THE VENTILATOR AND PLACED ON AN ALTERNATE VENTILATOR WITH NO HARM OR INJURY.

  Patient problems: No Code Available

  MAUDE report 7916047 ↗
• MalfunctionAug 31, 2018Failure to Power Up; No Flow; Failure to Power Up; No Flow

  ADDITIONAL INFORMATION RECEIVED AS FOLLOWS: IT WAS REPORTED THAT DURING SETTING UP THE 700 SERIES VENTILATOR PASSED POST (POWER ON SELF-TEST) WITH AN ERROR MESSAGE "IT COULD NOT BE USED". THE PATIENT WAS NOT ATTACHED TO THE VENTILATOR AT THE TIME OF THE EVENT. IMMEDIATELY ANOTHER VENTILATOR WAS PREPARED, AND IT WAS USED. NO HARM WAS REPORTED.

  Patient problems: No Code Available; No Patient Involvement

  MAUDE report 7839994 ↗
• MalfunctionAug 24, 2018No Flow; No Flow

  IT WAS REPORTED THAT DURING USE ON A PATIENT, THE SAFETY VALVE OPENED AND A ERROR MESSAGE WAS GENERATED. THE PATIENT WAS REMOVED FROM THE VENTILATOR AND PLACED ON AN ALTERNATE VENTILATOR.

  Patient problems: No Code Available

  MAUDE report 7814465 ↗
• MalfunctionAug 13, 2018No Flow; No Flow

  IT WAS REPORTED THAT DURING USE ON PATIENT THE 700 SERIES VENTILATOR SUDDEN SHUTDOWN. MANUAL VENTILATION WAS PERFORMED. THERE WAS ONLY ONE DEVICE THE CUSTOMER COULD USE SO THE TECHNICIAN RECHARGED THE BATTERY. THE VENTILATOR PASSED THE BATTERY LOAD TEST AFTER CHARGING. THE DEVICE IS CONTINUOUSLY BEING USED. NO PATIENT HARM WAS REPORTED.

  Patient problems: No Code Available

  MAUDE report 7778999 ↗
• MalfunctionJul 3, 2018Defective Component; Defective Component

  IT WAS REPORTED THAT DURING USE ON PATIENT 760 VENTILATOR HAD POST FAILED. THE DEVICE WAS REPLACED. NO PATIENT HARM REPORTED.

  Patient problems: No Code Available

  MAUDE report 7661179 ↗