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

Model Number 27083

Device Problem Inappropriate Tactile Prompt/Feedback (4023)

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

Event Date 06/20/2023

Event Type  malfunction  

Manufacturer Narrative

The main circuit board was replaced to address the reported complaint.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 (b)(4).

Event Description

During resmed evaluation, the right side of an astral device touchscreen was unresponsive.There was no patient harm or serious injury reported as a result of this incident.

• Brand Name: ASTRAL 150 - APAC
• Type of Device: VENTILATOR, CONTINUOUS (FACILITY/HOME)
• Manufacturer (Section D): RESMED PTY LTD; 1 elizabeth macarthur drive; bella vista; sydney, nsw 2153 ; AS 2153
• Manufacturer (Section G): RESMED PTY LTD; 1 elizabeth macarthur drive; bella vista; sydney, nsw 2153 ; AS 2153
• Manufacturer Contact: jaklin aziz ; 1 elizabeth macarthur drive; bella vista; sydney, nsw 2153 ; AS 2153
• MDR Report Key: 18241103
• MDR Text Key: 329449440
• Report Number: 3004604967-2023-00659
• Device Sequence Number: 1
• Product Code: NOU
• UDI-Device Identifier: 00619498270835
• UDI-Public: (01)00619498270835(11)170322(10)1230626
• Combination Product (y/n): N
• Reporter Country Code: AS
• PMA/PMN Number: K172875
• Number of Events Reported: 1
• Summary Report (Y/N): N
• Report Source: Manufacturer
• Source Type: Foreign
• Reporter Occupation: Other Health Care Professional
• Type of Report: Initial
• Report Date: 11/30/2023

1 Device was Involved in the Event

1 Patient was Involved in the Event

• Date FDA Received: 11/30/2023
• Is this an Adverse Event Report?: No
• Is this a Product Problem Report?: Yes
• Device Operator: Lay User/Patient
• Device Model Number: 27083
• Device Catalogue Number: 27083
• Was Device Available for Evaluation?: Device Returned to Manufacturer
• Date Returned to Manufacturer: 06/28/2023
• Is the Reporter a Health Professional?: Yes
• Distributor Facility Aware Date: 10/31/2023
• Date Manufacturer Received: 10/31/2023
• Was Device Evaluated by Manufacturer?: Yes
• Date Device Manufactured: 03/26/2017
• Is This a Reprocessed and Reused Single-Use Device?: No
• Type of Device Usage: A
• Patient Sequence Number: 1