MAUDE Adverse Event Report: RESMED PTY LTD ASTRAL 150 - DEU; VENTILATOR, CONTINUOUS (FACILITY/HOME)

Model Number 27053

Device Problems Charging Problem (2892); Complete Loss of Power (4015)

Patient Problem No Clinical Signs, Symptoms or Conditions (4582)

Event Date 11/06/2023

Event Type  malfunction  

Manufacturer Narrative

The device was returned to resmed and an evaluation confirmed the complaint.The power supply unit was replaced to address the issues.The device was serviced and fully tested before it was returned to the customer.Resmed reference#: (b)(4).

Event Description

It was reported to resmed that an astral device failed to charge its internal battery and shutdown unexpectedly.There was no patient harm or serious injury reported as a result of this incident.

Event Description

It was reported to resmed that an astral device failed to charge its internal battery and shutdown unexpectedly.There was no patient harm or serious injury reported as a result of this incident.

Manufacturer Narrative

The astral device was returned to resmed for an investigation.Review of the device data logs confirmed error messages (sf180) related to a battery charger fault and revealed the device shutdown due to a flat battery.Based on all available evidence and complaint investigations of a similar nature, the investigation determined sf180 was due to the device operating in high ambient temperatures.Resmed¿s risk analysis for this failure mode concludes that the risk is acceptable.Resmed reference#: (b)(4).

• Brand Name: ASTRAL 150 - DEU
• Type of Device: VENTILATOR, CONTINUOUS (FACILITY/HOME)
• Manufacturer (Section D): RESMED PTY LTD; 1 elizabeth macarthur drive; bella vista; sydney, nsw 2153 ; AS 2153
• MDR Report Key: 18331996
• MDR Text Key: 330554814
• Report Number: 3007573469-2023-00679
• Device Sequence Number: 1
• Product Code: NOU
• UDI-Device Identifier: 00619498270538
• UDI-Public: (01)00619498270538(10)1443711
• Combination Product (y/n): N
• Reporter Country Code: GM
• Number of Events Reported: 1
• Summary Report (Y/N): N
• Report Source: Distributor
• Reporter Occupation: Other Health Care Professional
• Type of Report: Initial,Followup
• Report Date: 04/25/2024

1 Device was Involved in the Event

1 Patient was Involved in the Event

• Is this an Adverse Event Report?: No
• Is this a Product Problem Report?: Yes
• Device Operator: Lay User/Patient
• Device Model Number: 27053
• Device Catalogue Number: 27053
• Was Device Available for Evaluation?: Device Returned to Manufacturer
• Date Returned to Manufacturer: 11/17/2023
• Is the Reporter a Health Professional?: Yes
• Was the Report Sent to FDA?: Yes
• Date Report Sent to FDA: 04/25/2024
• Distributor Facility Aware Date: 03/27/2024
• Device Age: 43 MO
• Date Report to Manufacturer: 04/25/2024
• Initial Date Manufacturer Received: Not provided
• Initial Date FDA Received: 12/14/2023
• Supplement Dates Manufacturer Received: 03/27/2024
• Supplement Dates FDA Received: 04/25/2024
• Was Device Evaluated by Manufacturer?: Yes
• Date Device Manufactured: 03/22/2020
• Is This a Reprocessed and Reused Single-Use Device?: No
• Type of Device Usage: A
• Patient Sequence Number: 1