ASTRAL 150 - AMER 27003

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2020-01-13 for ASTRAL 150 - AMER 27003 manufactured by Resmed Ltd.

Event Text Entries

[188703182] Resmed has requested for the device to be returned so that an engineering investigation could be performed. The device has not been returned, therefore resmed is unable to confirm the alleged malfunction at this time. Resmed reference #: (b)(4).
Patient Sequence No: 1, Text Type: N, H10


[188703183] It was reported to resmed an astral device displayed a battery error message. There was no patient harm or serious injury reported as a result of this incident.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number3007573469-2020-00146
MDR Report Key9583694
Date Received2020-01-13
Date of Report2020-02-26
Date Facility Aware2020-01-30
Report Date2020-02-26
Date Reported to FDA2020-02-26
Date Reported to Mfgr2020-02-26
Date Mfgr Received2020-01-30
Date Added to Maude2020-01-13
Event Key0
Report Source CodeDistributor report
Manufacturer LinkN
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag3
Reporter OccupationOTHER HEALTH CARE PROFESSIONAL
Health Professional3
Initial Report to FDA3
Report to FDA3
Event Location3
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameASTRAL 150 - AMER
Product CodeNOU
Date Received2020-01-13
Returned To Mfg2020-01-15
Model Number27003
Catalog Number27003
OperatorLAY USER/PATIENT
Device AvailabilityR
Device Age9 MO
Device Eval'ed by MfgrY
Device Sequence No1
Device Event Key0
ManufacturerRESMED LTD
Manufacturer Address1 ELIZABETH MACARTHUR DRIVE. BELLA VISTA SYDNEY, NSW 2153 AU 2153


Patients

Patient NumberTreatmentOutcomeDate
10 2020-01-13

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