Garbin 00Recalls & reported problems
Respironics, Inc. · Garbin Ventilator (Trilogy 100) · Class 2
Quick summary
This Respironics ventilator provides breathing support. The 63 reports mostly describe incorrect messages, battery problems, failure to charge, and devices not working as expected; most reports mention no patient involvement. They 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
- 63
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 63 adverse event reports that list this exact device (DI 00606959022768), received between Oct 14, 2015 and Jul 24, 2023 — classified as 63 malfunctions.
The most frequently reported specific device problem is “Device Displays Incorrect Message” (40 reports).
8 other recalls cover devices cleared under the same FDA submission (K083526); they may or may not involve this specific model.
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
Device problems
- Device Displays Incorrect Message40
- Battery Problem24
- Failure to Charge6
- Device Operates Differently Than Expected4
- Degraded2
- Device Operational Issue2
- Device Inoperable1
- Failure To Run On AC/DC1
Patient problems
- No Patient Involvement56
- No Consequences Or Impact To Patient3
- Cough2
- Headache2
- No Known Impact Or Consequence To Patient2
- Unspecified Respiratory Problem2
- Chest Pain1
- Eye Irritation1
Recent adverse event reports
The 25 most recent of 63 reports, in the reporter's own words as published by the FDA.
MalfunctionJul 24, 2023Degraded; Degraded
THE MANUFACTURER RECEIVED INFORMATION ALLEGING THAT A PATIENT EXPERIENCED VERTIGO, LIGHTHEADEDNESS, HEADACHE, COUGH, AND CHEST PRESSURE, IRRITATION AND DRYNESS OF THE RESPIRATORY TRACT, NOSE AND EYES WHEN USING A VENTILATOR. IN ADDITION, THE PATIENT ALLEGED EXPERIENCING AN "ACID" SMELL. NO MEDICAL INTERVENTION WAS REPORTED. THE MANUFACTURER'S INVESTIGATION IS ONGOING. A FOLLOW-UP REPORT WILL BE SUBMITTED WHEN THE MANUFACTURER'S INVESTIGATION IS COMPLETE.
Patient problems: Cough; Headache; Unspecified Respiratory Problem
MAUDE report 17379099 ↗MalfunctionJul 20, 2023Degraded; Degraded
THE MANUFACTURER WAS CONTACTED IN REFERENCE TO THE VOLUNTARY FIELD SAFETY NOTICE / RECALL NOTIFICATION RELATED TO THE SOUND ABATEMENT FOAM IN CERTAIN CPAP, BIPAP, AND MECHANICAL VENTILATOR DEVICES. THE MANUFACTURER RECEIVED INFORMATION ALLEGING VERTIGO, LIGHTHEADEDNESS, HEADACHE, COUGH, CHEST PRESSURE, IRRITATION AND DRYNESS OF THE RESPIRATORY TRACT, NOSE AND EYES, AS WELL AS SMELLING ACID SMELLS. THERE IS NO ALLEGATION OF SERIOUS OR PERMANENT HARM OR INJURY. NO MEDICAL INTERVENTION WAS REQUIRED BY THE PATIENT. THE MANUFACTURER'S INVESTIGATION IS ONGOING. A FOLLOW-UP REPORT WILL BE SUBMITTED WHEN THE MANUFACTURER'S INVESTIGATION IS COMPLETE.
Patient problems: Chest Pain; Cough; Eye Irritation; Headache; Unspecified Respiratory Problem; Vertigo
MAUDE report 17361317 ↗MalfunctionMar 14, 2018Device Operational Issue; Device Operational Issue
A VENTILATOR WAS RETURNED TO THE MANUFACTURER FOR SERVICE. THE DEVICE WAS NOT IN PATIENT USE. DURING THE EVALUATION OF THE DEVICE AT THE MANUFACTURER'S SERVICE CENTER, A "VENTILATOR INOPERATIVE" CODE WAS FOUND IN THE VENTILATOR'S DOWNLOADED ERROR LOG. THE DEVICE'S SYSTEM BOARD WAS REPLACED TO ADDRESS THE ISSUE.
Patient problems: No Patient Involvement
MAUDE report 7337453 ↗MalfunctionApr 26, 2017Device Inoperable; Device Displays Incorrect Message; Device Inoperable; Device Displays Incorrect Message
THE MANUFACTURER RECEIVED INFORMATION ALLEGING A VENTILATOR INOPERATIVE CONDITION OCCURRED. THERE WAS NO HARM OR INJURY REPORTED. THE VENTILATOR WAS RETURNED TO THE MANUFACTURER FOR EVALUATION AND THE CUSTOMER'S COMPLAINT WAS CONFIRMED. THE DEVICE'S SYSTEM BOARD WAS REPLACED TO ADDRESS THE ISSUE.
Patient problems: No Consequences Or Impact To Patient
MAUDE report 6521823 ↗MalfunctionApr 26, 2017Failure To Run On AC/DC; Failure To Run On AC/DC
THE MANUFACTURER RECEIVED INFORMATION ALLEGING A VENTILATOR WOULD NOT POWER ON. THERE WAS NO HARM OR INJURY REPORTED. THE VENTILATOR WAS RETURNED TO THE MANUFACTURER'S SERVICE CENTER FOR EVALUATION AND THE CUSTOMER'S COMPLAINT WAS CONFIRMED. THE DEVICE'S SYSTEM BOARD WAS REPLACED TO ADDRESS THE ISSUE.
Patient problems: No Patient Involvement
MAUDE report 6521815 ↗MalfunctionApr 26, 2017Device Displays Incorrect Message; Battery Problem; Device Displays Incorrect Message; Battery Problem
THE MANUFACTURER RECEIVED INFORMATION ALLEGING A VENTILATOR "SERVICE REQUIRED" ALARM CONDITION OCCURRED RELATED TO A FAILURE OF THE INTERNAL BATTERY. THE DEVICE WAS NOT IN PATIENT USE. THE VENTILATOR WAS RETURNED TO THE MANUFACTURER FOR EVALUATION AND THE CUSTOMER'S COMPLAINT WAS CONFIRMED. THE DEVICE'S INTERNAL BATTERY WAS REPLACED TO ADDRESS THE ISSUE.
Patient problems: No Patient Involvement
MAUDE report 6521811 ↗MalfunctionApr 26, 2017Device Displays Incorrect Message; Battery Problem; Device Displays Incorrect Message; Battery Problem
THE MANUFACTURER RECEIVED INFORMATION ALLEGING A VENTILATOR "SERVICE REQUIRED" ALARM CONDITION OCCURRED RELATED TO THE INTERNAL BATTERY. THERE WAS NO HARM OR INJURY REPORTED. THE VENTILATOR WAS RETURNED TO THE MANUFACTURER FOR EVALUATION AND THE CUSTOMER'S COMPLAINT WAS CONFIRMED. THE DEVICE'S INTERNAL BATTERY WAS REPLACED TO ADDRESS THE ISSUE.
Patient problems: No Consequences Or Impact To Patient
MAUDE report 6521809 ↗MalfunctionFeb 15, 2017Device Displays Incorrect Message; Battery Problem; Device Displays Incorrect Message; Battery Problem
THE MANUFACTURER RECEIVED INFORMATION ALLEGING A VENTILATOR "SERVICE REQUIRED" ALARM CONDITION OCCURRED RELATED TO A FAILURE OF ITS INTERNAL BATTERY. THE DEVICE WAS NOT IN PATIENT USE. THE VENTILATOR WAS RETURNED TO THE MANUFACTURER'S SERVICE CENTER FOR EVALUATION AND THE CUSTOMER'S COMPLAINT WAS CONFIRMED. THE DEVICE'S INTERNAL BATTERY WAS REPLACED TO ADDRESS THE ISSUES.
Patient problems: No Patient Involvement
MAUDE report 6332029 ↗MalfunctionFeb 15, 2017Device Displays Incorrect Message; Battery Problem; Device Displays Incorrect Message; Battery Problem
THE MANUFACTURER RECEIVED INFORMATION ALLEGING A VENTILATOR "SERVICE REQUIRED" ALARM CONDITION OCCURRED RELATED TO A FAILURE OF ITS INTERNAL BATTERY. THE DEVICE WAS NOT IN PATIENT USE. THE VENTILATOR WAS RETURNED TO THE MANUFACTURER'S SERVICE CENTER FOR EVALUATION AND THE CUSTOMER'S COMPLAINT WAS CONFIRMED. THE DEVICE'S INTERNAL BATTERY WAS REPLACED TO ADDRESS THE ISSUES.
Patient problems: No Patient Involvement
MAUDE report 6332028 ↗MalfunctionDec 21, 2016Device Displays Incorrect Message; Battery Problem; Device Displays Incorrect Message; Battery Problem
THE MANUFACTURER RECEIVED INFORMATION ALLEGING A VENTILATOR "SERVICE REQUIRED" ALARM CONDITION OCCURRED AND A FAILURE OF ITS INTERNAL BATTERY. THE DEVICE WAS NOT IN PATIENT USE. THE VENTILATOR WAS RETURNED TO THE MANUFACTURER FOR EVALUATION AND THE CUSTOMER'S COMPLAINT WAS CONFIRMED. THE DEVICE'S INTERNAL BATTERY WAS REPLACED TO ADDRESS THE ISSUE.
Patient problems: No Patient Involvement
MAUDE report 6193082 ↗MalfunctionDec 7, 2016Device Operational Issue; Device Operational Issue
THE MANUFACTURER RECEIVED INFORMATION ALLEGING AN ISSUE RELATED TO THE DEVICE'S SYSTEM BOARD. THE DEVICE WAS NOT IN PATIENT USE. 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 SYSTEM BOARD WAS REPLACED TO ADDRESS THE ISSUE.
Patient problems: No Patient Involvement
MAUDE report 6151567 ↗MalfunctionDec 7, 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. THE VENTILATOR WAS RETURNED TO THE MANUFACTURER FOR EVALUATION AND AN ERROR CODE RELATED TO THE CHARGING OF THE INTERNAL BATTERY WAS OBSERVED. THE DEVICE'S INTERNAL BATTERY WAS REPLACED TO ADDRESS THE ISSUE.
Patient problems: No Patient Involvement
MAUDE report 6151394 ↗MalfunctionDec 7, 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. THE VENTILATOR WAS RETURNED TO THE MANUFACTURER FOR EVALUATION AND AN ERROR CODE RELATED TO THE CHARGING OF THE INTERNAL BATTERY WAS OBSERVED. THE DEVICE'S INTERNAL BATTERY WAS REPLACED TO ADDRESS THE ISSUE.
Patient problems: No Patient Involvement
MAUDE report 6151384 ↗MalfunctionNov 15, 2016Device Displays Incorrect Message; Battery Problem; Device Displays Incorrect Message; Battery Problem
THE MANUFACTURER RECEIVED INFORMATION ALLEGING A VENTILATOR "SERVICE REQUIRED" ALARM CONDITION OCCURRED AND A FAILURE OF ITS INTERNAL BATTERY. THE DEVICE WAS NOT IN PATIENT USE. DURING THE EVALUATION OF THE DEVICE AT THE MANUFACTURER'S SERVICE CENTER, AN ERROR CODE RELATED TO THE CHARGING OF THE INTERNAL BATTERY WAS OBSERVED. THE DEVICE'S INTERNAL BATTERY WAS REPLACED TO ADDRESS THE ISSUE.
Patient problems: No Patient Involvement
MAUDE report 6102287 ↗MalfunctionNov 2, 2016Device Displays Incorrect Message; Battery Problem; Device Displays Incorrect Message; Battery Problem
THE MANUFACTURER RECEIVED INFORMATION ALLEGING A VENTILATOR "SERVICE REQUIRED" ALARM CONDITION OCCURRED AND A FAILURE OF ITS INTERNAL BATTERY. THE DEVICE WAS NOT IN PATIENT USE. DURING THE EVALUATION OF THE DEVICE AT THE MANUFACTURER'S SERVICE CENTER, AN ERROR CODE RELATED TO THE CHARGING OF THE INTERNAL BATTERY WAS OBSERVED. THE DEVICE'S INTERNAL BATTERY WAS REPLACED TO ADDRESS THE ISSUE.
Patient problems: No Patient Involvement
MAUDE report 6073718 ↗MalfunctionOct 12, 2016Failure to Power Up; Failure to Power Up
THE MANUFACTURER RECEIVED INFORMATION ALLEGING A VENTILATOR WOULD NOT POWER ON. THE DEVICE WAS NOT IN PATIENT USE. THE VENTILATOR WAS RETURNED TO THE MANUFACTURER FOR EVALUATION AND THE CUSTOMER'S COMPLAINT WAS CONFIRMED. THE DEVICE'S POWER SUPPLY WAS REPLACED TO ADDRESS THE ISSUE.
Patient problems: No Patient Involvement
MAUDE report 6021515 ↗MalfunctionOct 12, 2016Device Displays Incorrect Message; Device Displays Incorrect Message
THE MANUFACTURER RECEIVED INFORMATION ALLEGING A "SERVICE REQUIRED" ALARM CONDITION OCCURRED. THE DEVICE WAS NOT IN PATIENT USE. THE VENTILATOR WAS RETURNED TO THE MANUFACTURER FOR EVALUATION AND AN ERROR CODE RELATED TO THE CHARGING OF THE INTERNAL BATTERY WAS OBSERVED. THE DEVICE'S INTERNAL BATTERY WAS REPLACED TO ADDRESS THE ISSUE.
Patient problems: No Patient Involvement
MAUDE report 6021504 ↗MalfunctionOct 5, 2016Device Displays Incorrect Message; Device Displays Incorrect Message
THE MANUFACTURER RECEIVED INFORMATION ALLEGING A "SERVICE REQUIRED" ALARM CONDITION OCCURRED. THE DEVICE WAS NOT IN PATIENT USE. DURING THE EVALUATION OF THE DEVICE AT THE MANUFACTURER'S SERVICE CENTER, AN ERROR CODE RELATED TO THE CHARGING OF THE INTERNAL BATTERY WAS OBSERVED. THE DEVICE'S INTERNAL BATTERY WAS REPLACED TO ADDRESS THE ISSUE.
Patient problems: No Patient Involvement
MAUDE report 6000022 ↗MalfunctionOct 5, 2016Device Displays Incorrect Message; Device Displays Incorrect Message
THE MANUFACTURER RECEIVED INFORMATION ALLEGING A "SERVICE REQUIRED" ALARM CONDITION OCCURRED. THE DEVICE WAS NOT IN PATIENT USE. DURING THE EVALUATION OF THE DEVICE AT THE MANUFACTURER'S SERVICE CENTER, AN ERROR CODE RELATED TO THE CHARGING OF THE INTERNAL BATTERY WAS OBSERVED. THE DEVICE'S INTERNAL BATTERY WAS REPLACED TO ADDRESS THE ISSUE.
Patient problems: No Patient Involvement
MAUDE report 6000019 ↗MalfunctionOct 5, 2016Device Displays Incorrect Message; Device Displays Incorrect Message
THE MANUFACTURER RECEIVED INFORMATION ALLEGING A "SERVICE REQUIRED" ALARM CONDITION OCCURRED. THE DEVICE WAS NOT IN PATIENT USE. DURING THE EVALUATION OF THE DEVICE AT THE MANUFACTURER'S SERVICE CENTER, AN ERROR CODE RELATED TO THE CHARGING OF THE INTERNAL BATTERY WAS OBSERVED. THE DEVICE'S INTERNAL BATTERY WAS REPLACED TO ADDRESS THE ISSUE.
Patient problems: No Patient Involvement
MAUDE report 6000017 ↗MalfunctionOct 5, 2016Device Displays Incorrect Message; Device Displays Incorrect Message
THE MANUFACTURER RECEIVED INFORMATION ALLEGING A "SERVICE REQUIRED" ALARM CONDITION OCCURRED. THE DEVICE WAS NOT IN PATIENT USE. DURING THE EVALUATION OF THE DEVICE AT THE MANUFACTURER'S SERVICE CENTER, AN ERROR CODE RELATED TO THE CHARGING OF THE INTERNAL BATTERY WAS OBSERVED. THE DEVICE'S INTERNAL BATTERY WAS REPLACED TO ADDRESS THE ISSUE.
Patient problems: No Patient Involvement
MAUDE report 6000014 ↗MalfunctionJul 20, 2016Device Operates Differently Than Expected; Device Operates Differently Than Expected
A VENTILATOR WAS RETURNED TO THE MANUFACTURER FOR SERVICE. THE DEVICE WAS NOT IN PATIENT USE. 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 Patient Involvement
MAUDE report 5808832 ↗MalfunctionJul 20, 2016Device Operates Differently Than Expected; Device Operates Differently Than Expected
A VENTILATOR WAS RETURNED TO THE MANUFACTURER FOR SERVICE. THE DEVICE WAS NOT IN PATIENT USE. 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 Patient Involvement
MAUDE report 5808830 ↗MalfunctionJul 20, 2016Device Operates Differently Than Expected; Device Operates Differently Than Expected
A VENTILATOR WAS RETURNED TO THE MANUFACTURER FOR SERVICE. THE DEVICE WAS NOT IN PATIENT USE. 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 Patient Involvement
MAUDE report 5808829 ↗MalfunctionJul 20, 2016Device Operates Differently Than Expected; Device Operates Differently Than Expected
A VENTILATOR WAS RETURNED TO THE MANUFACTURER FOR SERVICE. THE DEVICE WAS NOT IN PATIENT USE. 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 Patient Involvement
MAUDE report 5808828 ↗
Recalls under the same FDA submission
These recalls involve devices cleared under K083526. One submission often covers many models, so check the product and lot details in each record.
- Z-0882-2023 · Dec 7, 2022 · Open, ClassifiedPhilips Trilogy 100 Ventilator, Model Numbers 1054260, 1054096, U1054260, U1054260B, 1054260B, CA1054096B, BT1054260, 1054096B, R1054260, RSL1054260, CA1054096, R1054260B, R1054655
- Z-0884-2023 · Dec 7, 2022 · Open, ClassifiedPhilips Garbin Ventilator, Model Number 1058180B
- Z-1956-2021 · Jun 14, 2021 · Open, ClassifiedTrilogy 100, Trilogy 200, Garbin Plus, Aeris, LifeVent Continuous Ventilators.
- Z-1065-2016 · Jan 18, 2016 · TerminatedTrilogy 100, Trilogy 200, Trilogy O2, Trilogy 202, Trilogy EC, Garbin, Garbin Plus Trilogy 100, Trilogy 200, Garbin, Garbin plus provides continuous or intermittent ventilatory su
- Z-1143-2014 · Feb 11, 2014 · TerminatedTrilogy Ventilators The Respironics Trilogy 100 system provides continuous or intermittent ventilator support for the care of individuals who require mechanical ventilation. Trilog
- Z-2024-2012 · Apr 27, 2012 · TerminatedRespironics Trilogy 100, 200, and 202 Ventilators The Respironics Trilogy systems provides continuous or intermittent ventilatory support for the care of individuals who require m
- Z-0296-2012 · Oct 11, 2011 · TerminatedTrilogy 100, 200 and 202 Ventilators The device is intended to be used in home, institution/hospital, and portable applications such as wheelchairs and gurneys, and may be used fo
- Z-1896-2010 · Jun 10, 2010 · TerminatedTrilogy 100 Ventilator, Model/Catalog Number 1054260, U1054260 (Domestic). Philips Respironics, Monroeville, PA 15146. Provides continuous or intermittent ventilatory support for
Other Oximeter devices
- Trilogy Trilogy100 Ventilator, InternationalRespironics, Inc. · Oximeter8 deaths2,493 reports
- Trilogy Trilogy 202 Ventilator, United StatesRespironics, Inc. · Oximeter2 deaths1,594 reports
- HAMILTON-G5 159001Hamilton Medical AG · Oximeter18 deaths1,440 reports
- Trilogy Trilogy100 Ventilator, GermanyRespironics, Inc. · Oximeter696 reports
- Model EMV+ Vent, Army, MRI 799-EMVP-04Zoll Medical Corporation · Oximeter1 death605 reports
- Trilogy Evo, O2, Japan JP2100X16BRespironics, Inc. · Oximeter4 recalls5 deaths342 reports
- Model EMV+ Vent, Army, COMMERCIAL 799-EMVP-01-01Zoll Medical Corporation · Oximeter1 death497 reports
- HAMILTON-G5 159002Hamilton Medical AG · Oximeter3 deaths451 reports
Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.