MAUDE Adverse Event Report: RESMED LTD ASTRAL 150 - EUR3; VENTILATOR, CONTINUOUS (FACILITY/HOME)

Model Number 27033

Device Problems Electrical /Electronic Property Problem (1198); Battery Problem (2885); Protective Measures Problem (3015)

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

Event Date 04/28/2023

Event Type  malfunction  

Manufacturer Narrative

The device was returned to resmed for evaluation.During resmed evaluation of an astral device, review of the device error logs revealed error message (sf180) related to power/charging fault.The battery was replaced to address the issue.The device was serviced and fully tested before it was returned to the customer.Resmed's risk analysis for this failure mode concludes that the risk is acceptable.Resmed reference#: pr 2787800.

Event Description

During resmed evaluation of an astral device, error message (sf180) related to power/charging fault was identified the device error logs there was no patient harm or serious injury reported as a result of this incident.

• Brand Name: ASTRAL 150 - EUR3
• Type of Device: VENTILATOR, CONTINUOUS (FACILITY/HOME)
• Manufacturer (Section D): RESMED LTD; 1 elizabeth macarthur drive; bella vista; sydney, nsw 2153 ; AS 2153
• MDR Report Key: 17760590
• MDR Text Key: 323578756
• Report Number: 3007573469-2023-00509
• Device Sequence Number: 1
• Product Code: NOU
• UDI-Device Identifier: 00619498270330
• UDI-Public: (01)00619498270330(10)1445594
• Combination Product (y/n): N
• Reporter Country Code: FR
• Number of Events Reported: 1
• Summary Report (Y/N): N
• Report Source: Distributor
• Reporter Occupation: Other Health Care Professional
• Type of Report: Initial
• Report Date: 09/14/2023

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: 27033
• Device Catalogue Number: 27033
• Was Device Available for Evaluation?: Device Returned to Manufacturer
• Date Returned to Manufacturer: 05/04/2023
• Is the Reporter a Health Professional?: Yes
• Was the Report Sent to FDA?: Yes
• Date Report Sent to FDA: 09/14/2023
• Distributor Facility Aware Date: 08/24/2023
• Device Age: 40 MO
• Date Report to Manufacturer: 09/14/2023
• Initial Date Manufacturer Received: Not provided
• Initial Date FDA Received: 09/15/2023
• Was Device Evaluated by Manufacturer?: Yes
• Date Device Manufactured: 04/01/2020
• Is This a Reprocessed and Reused Single-Use Device?: No
• Type of Device Usage: A
• Patient Sequence Number: 1