ASTRAL 27919Recalls & reported problems
Resmed Pty Ltd · ASTRAL EXTERNAL BATTERY · Class 2
All models of Astral (3)
Data updated Oct 16, 2026 from official FDA records · Editorial policy
Quick summary
This is the ResMed Astral external battery, a home-use ventilator accessory. The 27 reports mostly describe the battery running down faster than expected, showing battery error messages, or failing to charge, with no patient involvement or harm noted. There are no deaths and no injuries, and 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
- 27
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 27 adverse event reports that list this exact device (DI 00619498279197), received between Aug 23, 2017 and Jan 13, 2026 — classified as 27 malfunctions.
The most frequently reported specific device problem is “Premature Discharge of Battery” (13 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 16, 2026.
Reports received per month
Most reported problems
Device problems
- Premature Discharge of Battery13
- Battery Problem6
- Failure to Charge5
- Charging Problem2
- Protective Measures Problem2
- Defective Device1
- Power Problem1
Patient problems
- No Clinical Signs, Symptoms or Conditions14
- No Consequences Or Impact To Patient13
Recent adverse event reports
The 25 most recent of 27 reports, in the reporter's own words as published by the FDA.
MalfunctionJan 13, 2026Battery Problem
IT WAS REPORTED TO RESMED THAT AN ASTRAL DEVICE EXTERNAL BATTERY DISPLAYED A BATTERY ERROR MESSAGE. THERE WAS NO PATIENT INVOLVEMENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24058959 ↗MalfunctionJan 13, 2026Battery Problem
IT WAS REPORTED TO RESMED THAT AN ASTRAL DEVICE EXTERNAL BATTERY DISPLAYED A BATTERY ERROR MESSAGE. THERE WAS NO PATIENT INVOLVEMENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24058954 ↗MalfunctionJun 6, 2024Premature Discharge of Battery; Premature Discharge of Battery
IT WAS REPORTED TO RESMED THAT AN ASTRAL DEVICE HAD AN EXTERNAL BATTERY WITH A REDUCED LEVEL OF CAPACITY. THERE WAS NO PATIENT HARM OR SERIOUS INJURY REPORTED AS A RESULT OF THIS INCIDENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 19480989 ↗MalfunctionJun 6, 2024Premature Discharge of Battery; Premature Discharge of Battery
IT WAS REPORTED TO RESMED THAT AN ASTRAL DEVICE HAD AN EXTERNAL BATTERY WITH A REDUCED LEVEL OF CAPACITY. THERE WAS NO PATIENT HARM OR SERIOUS INJURY REPORTED AS A RESULT OF THIS INCIDENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 19480988 ↗MalfunctionJun 6, 2024Premature Discharge of Battery; Premature Discharge of Battery
IT WAS REPORTED TO RESMED THAT AN ASTRAL DEVICE HAD AN EXTERNAL BATTERY WITH A REDUCED LEVEL OF CAPACITY. THERE WAS NO PATIENT HARM OR SERIOUS INJURY REPORTED AS A RESULT OF THIS INCIDENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 19480985 ↗MalfunctionJun 6, 2024Premature Discharge of Battery; Premature Discharge of Battery
IT WAS REPORTED TO RESMED THAT AN ASTRAL DEVICE HAD AN EXTERNAL BATTERY WITH A REDUCED LEVEL OF CAPACITY. THERE WAS NO PATIENT HARM OR SERIOUS INJURY REPORTED AS A RESULT OF THIS INCIDENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 19480984 ↗MalfunctionJul 20, 2023Battery Problem; Battery Problem
IT WAS REPORTED TO RESMED THAT AN ASTRAL DEVICE EXTERNAL BATTERY HAD DEPLETED QUICKLY. THERE WAS NO PATIENT HARM OR SERIOUS INJURY REPORTED AS A RESULT OF THIS INCIDENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 17364467 ↗MalfunctionJul 20, 2023Battery Problem; Battery Problem
IT WAS REPORTED TO RESMED THAT AN ASTRAL DEVICE EXTERNAL BATTERY HAD DEPLETED QUICKLY. THERE WAS NO PATIENT HARM OR SERIOUS INJURY REPORTED AS A RESULT OF THIS INCIDENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 17364460 ↗MalfunctionNov 30, 2022Failure to Charge; Protective Measures Problem; Failure to Charge; Protective Measures Problem
IT WAS REPORTED TO RESMED THAT AN ASTRAL DEVICE FAILED TO CHARGE ITS EXTERNAL BATTERY AND DISPLAYED A BATTERY ERROR MESSAGE WHEN THE EXTERNAL BATTERY WAS CONNECTED TO THE DEVICE. THERE WAS NO PATIENT HARM OR SERIOUS INJURY REPORTED AS A RESULT OF THIS INCIDENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 15889902 ↗MalfunctionNov 30, 2022Failure to Charge; Protective Measures Problem; Failure to Charge; Protective Measures Problem
IT WAS REPORTED TO RESMED THAT AN ASTRAL DEVICE FAILED TO CHARGE ITS EXTERNAL BATTERY AND DISPLAYED A BATTERY ERROR MESSAGE WHEN THE EXTERNAL BATTERY WAS CONNECTED TO THE DEVICE. THERE WAS NO PATIENT HARM OR SERIOUS INJURY REPORTED AS A RESULT OF THIS INCIDENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 15889742 ↗MalfunctionNov 17, 2022Premature Discharge of Battery; Premature Discharge of Battery
IT WAS REPORTED TO RESMED THAT AN ASTRAL DEVICE HAD AN EXTERNAL BATTERY WITH A REDUCED LEVEL OF CAPACITY. THE DEVICE WAS NOT IN PATIENT USE WHEN THE REPORTED EVENT OCCURRED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 15819666 ↗MalfunctionNov 17, 2022Premature Discharge of Battery; Premature Discharge of Battery
IT WAS REPORTED TO RESMED THAT AN ASTRAL DEVICE HAD AN EXTERNAL BATTERY WITH A REDUCED LEVEL OF CAPACITY. THE DEVICE WAS NOT IN PATIENT USE WHEN THE REPORTED EVENT OCCURRED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 15818454 ↗MalfunctionJan 19, 2022Failure to Charge
IT WAS REPORTED TO RESMED THAT AN ASTRAL DEVICE FAILED TO CHARGE ITS INTERNAL BATTERY. THE DEVICE WAS NOT IN PATIENT USE WHEN THE REPORTED EVENT OCCURRED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 13290800 ↗MalfunctionJan 19, 2022Failure to Charge
IT WAS REPORTED TO RESMED THAT AN ASTRAL DEVICE FAILED TO CHARGE ITS INTERNAL BATTERY. THE DEVICE WAS NOT IN PATIENT USE WHEN THE REPORTED EVENT OCCURRED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 13290798 ↗MalfunctionSep 1, 2020Defective Device
IT WAS REPORTED TO RESMED THAT AN ASTRAL DEVICE HAD A DEFECTIVE EXTERNAL BATTERY. THERE WAS NO PATIENT HARM OR A SERIOUS INJURY REPORTED A AS A RESULT OF THE INCIDENT.
Patient problems: No Consequences Or Impact To Patient
MAUDE report 10480690 ↗MalfunctionSep 1, 2020Battery Problem
IT WAS REPORTED TO RESMED THAT AN ASTRAL DEVICE HAD A DEFECTIVE EXTERNAL BATTERY. THERE WAS NO PATIENT HARM OR A SERIOUS INJURY REPORTED A AS A RESULT OF THE INCIDENT.
Patient problems: No Consequences Or Impact To Patient
MAUDE report 10480689 ↗MalfunctionJan 7, 2020Premature Discharge of Battery; Premature Discharge of Battery
IT WAS REPORTED TO RESMED THAT AN ASTRAL DEVICE HAD AN EXTERNAL BATTERY WITH A REDUCED LEVEL OF CAPACITY. THERE WAS NO PATIENT HARM OR SERIOUS INJURY REPORTED AS A RESULT OF THIS INCIDENT.
Patient problems: No Consequences Or Impact To Patient
MAUDE report 9560895 ↗MalfunctionJan 7, 2020Premature Discharge of Battery; Premature Discharge of Battery
IT WAS REPORTED TO RESMED THAT AN ASTRAL DEVICE HAD AN EXTERNAL BATTERY WITH A REDUCED LEVEL OF CAPACITY. THERE WAS NO PATIENT HARM OR SERIOUS INJURY REPORTED AS A RESULT OF THIS INCIDENT.
Patient problems: No Consequences Or Impact To Patient
MAUDE report 9560829 ↗MalfunctionAug 27, 2019Premature Discharge of Battery; Premature Discharge of Battery
IT WAS REPORTED TO RESMED THAT AN ASTRAL DEVICE HAD AN EXTERNAL BATTERY WITH A REDUCED LEVEL OF CAPACITY. THERE WAS NO PATIENT HARM OR SERIOUS INJURY REPORTED AS A RESULT OF THIS INCIDENT.
Patient problems: No Consequences Or Impact To Patient
MAUDE report 8938228 ↗MalfunctionAug 27, 2019Premature Discharge of Battery; Premature Discharge of Battery
IT WAS REPORTED TO RESMED THAT AN ASTRAL DEVICE HAD AN EXTERNAL BATTERY WITH A REDUCED LEVEL OF CAPACITY. THERE WAS NO PATIENT HARM OR SERIOUS INJURY REPORTED AS A RESULT OF THIS INCIDENT.
Patient problems: No Consequences Or Impact To Patient
MAUDE report 8938223 ↗MalfunctionAug 27, 2019Premature Discharge of Battery; Premature Discharge of Battery
IT WAS REPORTED TO RESMED THAT AN ASTRAL DEVICE HAD AN EXTERNAL BATTERY WITH A REDUCED LEVEL OF CAPACITY. THERE WAS NO PATIENT HARM OR SERIOUS INJURY REPORTED AS A RESULT OF THIS INCIDENT.
Patient problems: No Consequences Or Impact To Patient
MAUDE report 8938221 ↗MalfunctionAug 27, 2019Premature Discharge of Battery; Premature Discharge of Battery
IT WAS REPORTED TO RESMED THAT AN ASTRAL DEVICE HAD AN EXTERNAL BATTERY WITH A REDUCED LEVEL OF CAPACITY. THERE WAS NO PATIENT HARM OR SERIOUS INJURY REPORTED AS A RESULT OF THIS INCIDENT.
Patient problems: No Consequences Or Impact To Patient
MAUDE report 8938220 ↗MalfunctionApr 12, 2019Premature Discharge of Battery; Premature Discharge of Battery
IT WAS REPORTED TO RESMED THAT AN ASTRAL DEVICE HAD AN INTERNAL BATTERY WITH A REDUCED LEVEL OF CAPACITY. THERE WAS NO PATIENT HARM OR SERIOUS INJURY REPORTED AS A RESULT OF THIS INCIDENT.
Patient problems: No Consequences Or Impact To Patient
MAUDE report 8511888 ↗MalfunctionMar 26, 2019Failure to Charge; Failure to Charge
IT WAS REPORTED TO RESMED THAT AN ASTRAL EXTERNAL BATTERY WAS FAILING TO CHARGE. THERE WAS NO PATIENT HARM OR SERIOUS INJURY REPORTED AS A RESULT OF THIS INCIDENT.
Patient problems: No Consequences Or Impact To Patient
MAUDE report 8451205 ↗MalfunctionMar 22, 2018Battery Problem; Battery Problem
IT WAS REPORTED TO RESMED THAT AN ASTRAL DEVICE FAILED TO DETECT AN EXTERNAL POWER SOURCE AND WAS DEPLETING ITS INTERNAL BATTERY. THERE WAS NO PATIENT HARM OR SERIOUS INJURY REPORTED AS A RESULT OF THIS INCIDENT.
Patient problems: No Consequences Or Impact To Patient
MAUDE report 7360853 ↗
Other Continuous, Ventilator, Home Use devices
- Astral 150Resmed Pty Ltd · Continuous, Ventilator, Home Use1 recall17 deaths2,361 reports
- Trilogy EV300, USA DS2200X11BRespironics, Inc. · Continuous, ventilator, home use5 recalls2,071 reports
- Trilogy 00Respironics, Inc. · CONTINUOUS, VENTILATOR, HOME USE15 deaths2,059 reports
- Trilogy Evo, Japan JP2110X16BRespironics, Inc. · Continuous, ventilator, home use5 recalls27 deaths1,112 reports
- Astral 100Resmed Pty Ltd · Continuous, Ventilator, Home Use9 deaths865 reports
- Trilogy Trilogy Evo Ventilator, IntlRespironics, Inc. · CONTINUOUS, VENTILATOR, HOME USE4 recalls3 deaths648 reports
- Life2000 MS-01-0118Welch Allyn, Inc. · Continuous, ventilator, home use10 recalls2 reports
- Trilogy Evo GB2110X15BRespironics, Inc. · Continuous, ventilator, home use5 recalls1 death141 reports
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 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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