MAUDE Adverse Event Report: RESPIRONICS, INC. BIPAP AVAPS C SERIES ; VENTILATOR, CONTINUOUS, NON-LIFE-SUPPORTING

Model Number	1161T
Medical Device Problem Code	Degraded (1153)
Health Effect - Clinical Code	No Clinical Signs, Symptoms or Conditions (4582)
Date of Event	12/08/2014
Type of Reportable Event	Malfunction
Additional Manufacturer Narrative
This mdr is being submitted as part of a batch submission of complaints that were reassessed as reportable foam degradation complaints; discovered as part of a retrospective remediation review.
Event or Problem Description
The manufacturer received information alleging an issue related to the bipap device's sound abatement foam.There was no report of patient harm or injury.This issue was reported to the fda per 21 cfr 806.The device will be corrected per res 88058.
Additional Manufacturer Narrative
The manufacturer previously reported incorrect information alleging an issue related to the bipap device's sound abatement foam.There was no report of patient harm or injury.This issue was reported to the fda per 21 cfr 806.The device will be corrected per res 88058.Section b5 should have been reported as: a bipap was returned to the manufacturer for service.There was no patient harm or injury reported.During the evaluation of the device at the manufacturer's service center, the customer's complaints could not be duplicated.The blower housing, blower cap, right panel assembly, bellows, sound foam and air inlet seal were replaced due to preventative maintenance.Section e.1 was incorrectly reported in previous report, which is now updated in this follow-up report.
Additional Manufacturer Narrative
In previous report, the manufacturer reported the incorrect information in section b2 marked as death, after review, it was determined that there this options were incorrectly selected in section b2.Nothing such has occured to the patient.The following correction has been updated in this report.Section b1 has been updated to reflect as product problem.Section h1 has also been updated to reflect the malfunction.Section h6 health impact code has also been updated to reflect the no health consequences or impact.

• Brand Name: BIPAP AVAPS C SERIES
• Common Device Name: VENTILATOR, CONTINUOUS, NON-LIFE-SUPPORTING
• Manufacturer (Section D): RESPIRONICS, INC.; 1001 murry ridge lane; murrysville PA 15668
• Manufacturer (Section G): RESPIRONICS, INC.; 1001 murry ridge lane; murrysville PA 15668
• Manufacturer Contact: kimberly shelly ; 6501 living place; pittsburgh, PA 15206 ; 2673970028
• MDR Report Key: 13877915
• Report Number: 2518422-2022-11028
• Device Sequence Number: 17273137
• Product Code: MNS
• UDI-Device Identifier: 00606959039247
• UDI-Public: 00606959039247
• Combination Product (Y/N): N
• Initial Reporter Country: CA
• PMA/510(K) Number: K092818
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Serviced by Third Party (Y/N): Unknown
• Reporter Type: Manufacturer
• Report Source: Foreign,Consumer
• Initial Reporter Occupation: Non-Healthcare Professional
• Remedial Action: Recall
• Type of Report: Initial,Followup,Followup
• Report Date (Section B): 10/25/2023

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
• Operator of Device: Lay User/Patient
• Device Model Number: 1161T
• Device Catalogue Number: 1161T
• Was Device Available for Evaluation?: Device Returned to Manufacturer
• Date Returned to Manufacturer: 12/05/2014
• Type of Report(Section G): Thirty-Day
• Initial Date Received by Manufacturer: 12/08/2014
• Supplement Date Received by Manufacturer: 12/08/2014; 12/08/2014
• Initial Report FDA Received Date: 03/24/2022
• Supplement Report FDA Received Date: 09/02/2022; 10/25/2023
• Was Device Evaluated by Manufacturer? (Y/N): Yes
• Date Device Manufactured: 01/30/2014
• Is the Device Labeled for Single Use? (Y/N): No
• Is This a Single-Use Device that was Reprocessed and Reused on a Patient? (Y/N): No
• Usage of Device: Unknown
• If action reported to FDA under 21 USC 360i(g), list FDA-assigned Recall Number or include a statement: RES 88058
• Patient Sequence Number: 1
• Outcome Attributed to Adverse Event: Death
• Patient Sex: Unknown