Trilogy Trilogy200 Ventilator, Latin AmericaRecalls & reported problems
Respironics, Inc. · Trilogy 200 Ventilator, Latin America version · Class 2
All models of Philips Trilogy Ventilator (90) · Trilogy (46)
Data updated Oct 18, 2026 from official FDA records · Editorial policy
Quick summary
This Respironics Trilogy 200 ventilator is a home-use breathing ventilator. The 25 reports mostly describe battery charging problems and service-required alarms, with internal tubing, screens and other parts needing repair or replacement. The reports mention no deaths and no injuries. No recalls name this device.
AI-generated from the FDA records on this page and checked automatically against the numbers below. Read the details before relying on it.
- Adverse event reports
- 25
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 25 adverse event reports that list this exact device (DI 00606959022829), received between Mar 2, 2016 and Nov 26, 2024 — classified as 25 malfunctions.
The most frequently reported specific device problem is “Failure to Charge” (10 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.
Reports received per month
Most reported problems
Device problems
- Failure to Charge10
- Device Operates Differently Than Expected6
- Device Displays Incorrect Message4
- Charging Problem3
- Device Operational Issue3
- Appropriate Device Problem Term/Code Not Available2
- Battery Problem2
- Adverse Event Without Identified Device or Use Problem1
Patient problems
- No Consequences Or Impact To Patient20
- No Known Impact Or Consequence To Patient11
- No Patient Involvement3
- No Clinical Signs, Symptoms or Conditions2
Recent adverse event reports
The 25 most recent of 25 reports, in the reporter's own words as published by the FDA.
MalfunctionNov 26, 2024Battery Problem; Battery Problem
A VENTILATOR WAS RETURNED TO A THIRD-PARTY SERVICE CENTER FOR SERVICE. THERE WAS NO HARM OR INJURY REPORTED. DURING THE EVALUATION OF THE DEVICE AT THIRD-PARTY SERVICE CENTER, A "SERVICE REQUIRED" CODE WAS FOUND IN THE VENTILATOR'S DOWNLOADED ERROR LOG. THE DEVICE'S INTERNAL BATTERY WAS REPLACED TO ADDRESS THE ISSUE. ADDITIONAL FINDINGS NOT RELATED TO THE MALFUNCTION/ISSUE WAS THE FOLLOWING PARTS WERE PROACTIVELY ON THE DEVICE: SENSOR BOARD AND FILTER. IN ADDITION, THERE WAS NO EVIDENCE OF FOAM PARTICLES FOUND ON THE DEVICE. AFTER REPLACING THE PARTS ON THE DEVICE, A SYSTEM TEST WAS PERFORMED, WHICH PASSED ON THE DEVICE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 20788194 ↗MalfunctionJan 15, 2019Mechanical Problem; Application Program Problem; Mechanical Problem; Application Program Problem
THE MANUFACTURER RECEIVED INFORMATION ALLEGING A VENTILATOR INOPERATIVE CONDITION OCCURRED. THERE WAS NO HARM OR INJURY REPORTED. THE DEVICE HAS NOT YET BEEN RETURNED TO THE MANUFACTURER. AT THIS TIME, WE ARE UNABLE TO CONFIRM THE ALLEGED MALFUNCTION. A FOLLOW-UP REPORT WILL BE SUBMITTED WHEN THE MANUFACTURER'S INVESTIGATION IS COMPLETE.
Patient problems: No Consequences Or Impact To Patient
MAUDE report 8247979 ↗MalfunctionJan 10, 2018Device Operational Issue; Device Operational Issue
A VENTILATOR WAS RETURNED TO THE MANUFACTURER FOR SERVICE. THERE WAS NO HARM OR INJURY REPORTED. DURING THE EVALUATION OF THE DEVICE AT THE MANUFACTURER'S SERVICE CENTER, THE DEVICE'S EXHALATION PORTING BLOCK WAS FOUND TO BE DAMAGED. THE DEVICE'S EXHALATION PORTING BLOCK WAS REPLACED TO ADDRESS THE ISSUE. THE DEVICE HAD EVIDENCE OF PHYSICAL DAMAGE.
Patient problems: No Consequences Or Impact To Patient
MAUDE report 7178219 ↗MalfunctionAug 16, 2017Device Operational Issue; Device Operational Issue
THE MANUFACTURER RECEIVED INFORMATION ALLEGING A VENTILATOR WOULD NOT WORK WITH AN ACTIVE CIRCUIT. THERE WAS NO HARM OR INJURY REPORTED. DURING THE EVALUATION OF THE DEVICE AT THE MANUFACTURER'S SERVICE CENTER, THE INTERNAL TUBING WAS OBSERVED BY THE TECHNICIAN TO BE DISCONNECTED FROM THE SENSOR BOARD. THE TUBING WILL BE RECONNECTED TO ADDRESS THE ISSUE.
Patient problems: No Consequences Or Impact To Patient
MAUDE report 6796974 ↗MalfunctionApr 5, 2017Device Inoperable; Device Displays Incorrect Message; Device Operational Issue; Device Displays Incorrect Message; Device Operational Issue
THE MANUFACTURER RECEIVED INFORMATION ALLEGING A FAILURE OF A VENTILATOR'S BLOWER MOTOR. THERE WAS NO HARM OR INJURY REPORTED. THE DEVICE HAS YET TO BE RETURNED TO THE MANUFACTURER FOR EVALUATION. AT THIS TIME, WE ARE UNABLE TO CONFIRM THE ALLEGED MALFUNCTION. A FOLLOW-UP REPORT WILL BE SUBMITTED WHEN THE MANUFACTURER'S INVESTIGATION IS COMPLETE.
Patient problems: No Consequences Or Impact To Patient; No Known Impact Or Consequence To Patient
MAUDE report 6460095 ↗MalfunctionMar 8, 2017Failure to Charge; Device Displays Incorrect Message; Failure to Charge
THE MANUFACTURER RECEIVED INFORMATION ALLEGING A VENTILATOR "SERVICE REQUIRED" ALARM CONDITION OCCURRED RELATING TO A FAILURE TO CHARGE ITS INTERNAL BATTERY. THE DEVICE WAS NOT IN PATIENT USE. THE DEVICE HAS YET TO BE RETURNED TO THE MANUFACTURER FOR EVALUATION. AT THIS TIME, WE ARE UNABLE TO CONFIRM THE ALLEGED MALFUNCTION. A FOLLOW-UP REPORT WILL BE SUBMITTED WHEN THE MANUFACTURER'S INVESTIGATION IS COMPLETE.
Patient problems: No Patient Involvement
MAUDE report 6387321 ↗MalfunctionMar 8, 2017Failure to Charge; Device Displays Incorrect Message
THE MANUFACTURER RECEIVED INFORMATION ALLEGING A VENTILATOR "SERVICE REQUIRED" ALARM CONDITION OCCURRED RELATING TO A FAILURE TO CHARGE ITS INTERNAL BATTERY. THE DEVICE WAS NOT IN PATIENT USE. THE DEVICE HAS YET TO BE RETURNED TO THE MANUFACTURER FOR EVALUATION. AT THIS TIME, WE ARE UNABLE TO CONFIRM THE ALLEGED MALFUNCTION. A FOLLOW-UP REPORT WILL BE SUBMITTED WHEN THE MANUFACTURER'S INVESTIGATION IS COMPLETE.
Patient problems: No Patient Involvement
MAUDE report 6387318 ↗MalfunctionOct 12, 2016No Display/Image; Appropriate Device Problem Term/Code Not Available; No Display/Image; Appropriate Device Problem Term/Code Not Available
A VENTILATOR WAS RETURNED TO A THIRD PARTY SERVICE CENTER FOR EVALUATION. THE DEVICE WAS NOT IN PATIENT USE. DURING THE EVALUATION OF THE DEVICE AT A THIRD PARTY SERVICE CENTER, A FAILURE OF THE DEVICE'S LCD SCREEN WAS OBSERVED. THE DEVICE'S LCD SCREEN WAS REPLACED TO ADDRESS THE ISSUE. DURING THE EVALUATION OF THE DEVICE AT A THIRD PARTY SERVICE CENTER, A "SERVICE REQUIRED" CODE WAS FOUND IN THE VENTILATOR'S DOWNLOADED ERROR LOG. THE DEVICE'S POWER MANAGEMENT BOARD WAS REPLACED TO ADDRESS THE ISSUE.
Patient problems: No Patient Involvement
MAUDE report 6021516 ↗MalfunctionOct 6, 2016Adverse Event Without Identified Device or Use Problem; Device Operates Differently Than Expected; Adverse Event Without Identified Device or Use Problem
THE MANUFACTURER RECEIVED INFORMATION ALLEGING A VENTILATOR'S EXHALATION VALVE WAS NOT FUNCTIONING AS DESIGNED. THERE WAS NO HARM OR INJURY REPORTED. THE DEVICE HAS YET TO BE RETURNED TO THE MANUFACTURER FOR EVALUATION. AT THIS TIME, WE ARE UNABLE TO CONFIRM THE ALLEGED MALFUNCTION. A FOLLOW-UP REPORT WILL BE SUBMITTED WHEN THE MANUFACTURER'S INVESTIGATION IS COMPLETE.
Patient problems: No Consequences Or Impact To Patient; No Known Impact Or Consequence To Patient
MAUDE report 6002940 ↗MalfunctionSep 27, 2016Device Operates Differently Than Expected
THE MANUFACTURER RECEIVED INFORMATION ALLEGING A FAILURE OF THE VENTILATOR'S EXHALATION VALVE. THERE WAS NO HARM OR INJURY REPORTED. THE DEVICE HAS YET TO BE RETURNED TO THE MANUFACTURER FOR EVALUATION. AT THIS TIME, WE ARE UNABLE TO CONFIRM THE ALLEGED MALFUNCTION. A FOLLOW-UP REPORT WILL BE SUBMITTED WHEN THE MANUFACTURER'S INVESTIGATION IS COMPLETE.
Patient problems: No Known Impact Or Consequence To Patient
MAUDE report 5980556 ↗MalfunctionSep 14, 2016Charging Problem
THE MANUFACTURER RECEIVED INFORMATION ALLEGING A VENTILATOR HAD A CHARGING ISSUE. THERE WAS NO HARM OR INJURY REPORTED. THE DEVICE HAS YET TO BE RETURNED TO THE MANUFACTURER FOR EVALUATION. AT THIS TIME, WE ARE UNABLE TO CONFIRM THE ALLEGED MALFUNCTION. A FOLLOW-UP REPORT WILL BE SUBMITTED WHEN THE MANUFACTURER'S INVESTIGATION IS COMPLETE.
Patient problems: No Consequences Or Impact To Patient; No Known Impact Or Consequence To Patient
MAUDE report 5950009 ↗MalfunctionSep 14, 2016Failure to Charge; Charging Problem; Charging Problem
THE MANUFACTURER RECEIVED INFORMATION ALLEGING A VENTILATOR HAD A CHARGING ISSUE. THERE WAS NO HARM OR INJURY REPORTED. THE DEVICE HAS YET TO BE RETURNED TO THE MANUFACTURER FOR EVALUATION. AT THIS TIME, WE ARE UNABLE TO CONFIRM THE ALLEGED MALFUNCTION. A FOLLOW-UP REPORT WILL BE SUBMITTED WHEN THE MANUFACTURER'S INVESTIGATION IS COMPLETE.
Patient problems: No Consequences Or Impact To Patient; No Known Impact Or Consequence To Patient
MAUDE report 5949825 ↗MalfunctionSep 14, 2016Charging Problem
THE MANUFACTURER RECEIVED INFORMATION ALLEGING A VENTILATOR HAD A CHARGING ISSUE. THERE WAS NO HARM OR INJURY REPORTED. THE DEVICE HAS YET TO BE RETURNED TO THE MANUFACTURER FOR EVALUATION. AT THIS TIME, WE ARE UNABLE TO CONFIRM THE ALLEGED MALFUNCTION. A FOLLOW-UP REPORT WILL BE SUBMITTED WHEN THE MANUFACTURER'S INVESTIGATION IS COMPLETE.
Patient problems: No Consequences Or Impact To Patient; No Known Impact Or Consequence To Patient
MAUDE report 5949814 ↗MalfunctionAug 17, 2016Failure to Charge; Failure to Charge
A VENTILATOR WAS RETURNED TO A THIRD PARTY SERVICE CENTER FOR EVALUATION. THERE WAS NO HARM OR INJURY REPORTED. DURING THE EVALUATION OF THE DEVICE AT A THIRD PARTY SERVICE CENTER, A FAILURE OF THE DEVICE TO CHARGE ITS INTERNAL BATTERY WAS OBSERVED. THE DEVICE'S INTERNAL BATTERY WAS REPLACED TO ADDRESS THE ISSUE.
Patient problems: No Consequences Or Impact To Patient
MAUDE report 5883014 ↗MalfunctionAug 15, 2016Failure to Charge; Failure to Charge
A VENTILATOR WAS RETURNED TO A THIRD PARTY SERVICE CENTER FOR EVALUATION. THERE WAS NO HARM OR INJURY REPORTED. DURING THE EVALUATION OF THE VENTILATOR AT THE THIRD PARTY SERVICE CENTER, A FAILURE OF THE DEVICE TO CHARGE IT'S INTERNAL BATTERY WAS OBSERVED. THE DEVICE'S INTERNAL BATTERY WAS REPLACED TO ADDRESS THE ISSUE.
Patient problems: No Consequences Or Impact To Patient
MAUDE report 5876789 ↗MalfunctionAug 15, 2016Failure to Charge; Failure to Charge
A VENTILATOR WAS RETURNED TO A THIRD PARTY SERVICE CENTER FOR EVALUATION. THERE WAS NO HARM OR INJURY REPORTED. DURING THE EVALUATION OF THE VENTILATOR AT THE THIRD PARTY SERVICE CENTER, A FAILURE OF THE DEVICE TO CHARGE IT'S INTERNAL BATTERY WAS OBSERVED. THE DEVICE'S INTERNAL BATTERY WAS REPLACED TO ADDRESS THE ISSUE.
Patient problems: No Consequences Or Impact To Patient
MAUDE report 5876788 ↗MalfunctionJun 22, 2016Failure to Charge; Failure to Charge
A VENTILATOR WAS RETURNED TO A THIRD PARTY SERVICE CENTER FOR EVALUATION. THERE WAS NO HARM OR INJURY REPORTED. DURING THE EVALUATION OF THE DEVICE AT A THIRD PARTY SERVICE CENTER, A FAILURE OF THE DEVICE TO CHARGE ITS INTERNAL BATTERY WAS OBSERVED. THE DEVICE'S INTERNAL BATTERY WAS REPLACED TO ADDRESS THE ISSUE.
Patient problems: No Consequences Or Impact To Patient
MAUDE report 5741810 ↗MalfunctionJun 22, 2016Failure to Charge; Failure to Charge
A VENTILATOR WAS RETURNED TO A THIRD PARTY SERVICE CENTER FOR EVALUATION. THERE WAS NO HARM OR INJURY REPORTED. DURING THE EVALUATION OF THE DEVICE AT A THIRD PARTY SERVICE CENTER, A FAILURE OF THE DEVICE TO CHARGE ITS INTERNAL BATTERY WAS OBSERVED. THE DEVICE'S INTERNAL BATTERY WAS REPLACED TO ADDRESS THE ISSUE.
Patient problems: No Consequences Or Impact To Patient
MAUDE report 5741809 ↗MalfunctionJun 22, 2016Failure to Charge; Failure to Charge
A VENTILATOR WAS RETURNED TO A THIRD PARTY SERVICE CENTER FOR EVALUATION. THERE WAS NO HARM OR INJURY REPORTED. DURING THE EVALUATION OF THE DEVICE AT A THIRD PARTY SERVICE CENTER, A FAILURE OF THE DEVICE TO CHARGE ITS INTERNAL BATTERY WAS OBSERVED. THE DEVICE'S INTERNAL BATTERY WAS REPLACED TO ADDRESS THE ISSUE.
Patient problems: No Consequences Or Impact To Patient
MAUDE report 5741805 ↗MalfunctionMay 25, 2016Device Displays Incorrect Message; Device Displays Incorrect Message
THE MANUFACTURER RECEIVED INFORMATION ALLEGING A "SERVICE REQUIRED" ALARM CONDITION OCCURRED. THERE WAS NO HARM OR INJURY REPORTED. DURING THE EVALUATION OF THE DEVICE AT THE MANUFACTURER'S SERVICE CENTER, A "SERVICE REQUIRED" CODE WAS FOUND IN THE VENTILATOR'S DOWNLOADED ERROR LOG. THE DEVICE'S INTERNAL BATTERY WAS REPLACED TO ADDRESS THE ISSUE.
Patient problems: No Consequences Or Impact To Patient
MAUDE report 5678432 ↗MalfunctionMar 3, 2016Appropriate Device Problem Term/Code Not Available; Device Operates Differently Than Expected; Appropriate Device Problem Term/Code Not Available
THE MANUFACTURER RECEIVED INFORMATION FROM A THIRD PARTY SERVICE CENTER ALLEGING A VENTILATOR'S ACTIVE EXHALATION CONTROL VALVE REMAINED OPEN. THERE WAS NO REPORT OF PATIENT HARM OR INJURY. THE DEVICE HAS NOT YET BEEN EVALUATED BY THE MANUFACTURER. AT THIS TIME, WE ARE UNABLE TO CONFIRM THE ALLEGED MALFUNCTION. A FOLLOW-UP REPORT WILL BE SUBMITTED WHEN THE MANUFACTURER'S INVESTIGATION IS COMPLETE.
Patient problems: No Consequences Or Impact To Patient; No Known Impact Or Consequence To Patient
MAUDE report 5476611 ↗MalfunctionMar 2, 2016Battery Problem; Failure to Charge; Battery Problem
THE MANUFACTURER RECEIVED INFORMATION FROM A THIRD PARTY SERVICE CENTER ALLEGING A VENTILATOR'S INTERNAL BATTERY WAS NOT CHARGING. THERE WAS NO REPORT OF PATIENT HARM OR INJURY. THE DEVICE HAS NOT YET BEEN EVALUATED BY THE MANUFACTURER. AT THIS TIME, WE ARE UNABLE TO CONFIRM THE ALLEGED MALFUNCTION. A FOLLOW-UP REPORT WILL BE SUBMITTED WHEN THE MANUFACTURER'S INVESTIGATION IS COMPLETE.
Patient problems: No Consequences Or Impact To Patient; No Known Impact Or Consequence To Patient
MAUDE report 5475540 ↗MalfunctionMar 2, 2016Device Operates Differently Than Expected
THE MANUFACTURER RECEIVED INFORMATION ALLEGING A VENTILATOR'S ACTIVE EXHALATION CONTROL VALVE REMAINED OPEN. THERE WAS NO REPORT OF PATIENT HARM OR INJURY. THE DEVICE HAS NOT YET BEEN EVALUATED BY THE MANUFACTURER. AT THIS TIME, WE ARE UNABLE TO CONFIRM THE ALLEGED MALFUNCTION. A FOLLOW-UP REPORT WILL BE SUBMITTED WHEN THE MANUFACTURER'S INVESTIGATION IS COMPLETE.
Patient problems: No Consequences Or Impact To Patient; No Known Impact Or Consequence To Patient
MAUDE report 5475462 ↗MalfunctionMar 2, 2016Device Operates Differently Than Expected; Device Slipped; Device Operates Differently Than Expected
THE MANUFACTURER RECEIVED INFORMATION FROM A THIRD PARTY SERVICE CENTER ALLEGING A VENTILATOR'S ACTIVE EXHALATION CONTROL VALVE REMAINED OPEN. THERE WAS NO REPORT OF PATIENT HARM OR INJURY. THE DEVICE HAS NOT YET BEEN EVALUATED BY THE MANUFACTURER. AT THIS TIME, WE ARE UNABLE TO CONFIRM THE ALLEGED MALFUNCTION. A FOLLOW-UP REPORT WILL BE SUBMITTED WHEN THE MANUFACTURER'S INVESTIGATION IS COMPLETE.
Patient problems: No Consequences Or Impact To Patient; No Known Impact Or Consequence To Patient
MAUDE report 5474296 ↗MalfunctionMar 2, 2016Degraded; Degraded; Device Operates Differently Than Expected
THE MANUFACTURER RECEIVED INFORMATION FROM A THIRD PARTY SERVICE CENTER ALLEGING A VENTILATOR'S ACTIVE EXHALATION CONTROL VALVE REMAINED OPEN. THERE WAS NO REPORT OF PATIENT HARM OR INJURY. THE DEVICE HAS NOT YET BEEN EVALUATED BY THE MANUFACTURER. AT THIS TIME, WE ARE UNABLE TO CONFIRM THE ALLEGED MALFUNCTION. A FOLLOW-UP REPORT WILL BE SUBMITTED WHEN THE MANUFACTURER'S INVESTIGATION IS COMPLETE.
Patient problems: No Clinical Signs, Symptoms or Conditions; No Consequences Or Impact To Patient; No Known Impact Or Consequence To Patient
MAUDE report 5474283 ↗
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Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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