MAUDE Adverse Event Report: RESPIRONICS, INC. A40 SILVER SERIES; VENTILATOR, NON-CONTINUOUS (RESPIRATOR)

Model Number	1116153
Medical Device Problem Code	Degraded (1153)
Health Effect - Clinical Code	No Clinical Signs, Symptoms or Conditions (4582)
Date of Event	05/18/2016
Type of Reportable Event	Malfunction
Event or Problem Description
The manufacturer received information alleging an issue related to a cpap device's sound abatement foam.There was no report of patient harm or injury.The device was returned and the manufacturer has confirmed of defective blower.
Additional Manufacturer Narrative
The manufacturer previously reported wrong statement in section b5.The correct statement will be: the manufacturer received information alleging an issue related to a cpap device's sound abatement foam.There was no report of patient harm or injury.The device was returned and the manufacturer has confirmed of defective blower.This issue was reported to the fda per 21 cfr 806.The device will be corrected per res (b)(4).Also, previously in section h10, nothing was marked and written.Section h10 will be marked as manufacturer narrative and the statement will be: 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.

• Brand Name: A40 SILVER SERIES
• Common Device Name: VENTILATOR, NON-CONTINUOUS (RESPIRATOR)
• 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: 15200264
• Report Number: 2518422-2022-11386
• Device Sequence Number: 6413644
• Product Code: BZD
• UDI-Device Identifier: 00606959042834
• UDI-Public: 00606959042834
• Combination Product (Y/N): N
• Initial Reporter Country: GM
• PMA/510(K) Number: K131982
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Serviced by Third Party (Y/N): Unknown
• Reporter Type: Manufacturer
• Report Source: Foreign,User Facility
• Initial Reporter Occupation: Non-Healthcare Professional
• Remedial Action: Recall
• Type of Report: Initial,Followup
• Report Date (Section B): 08/19/2022

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: 1116153
• Device Catalogue Number: 1116153
• Was Device Available for Evaluation?: Yes
• Type of Report(Section G): Thirty-Day
• Initial Date Received by Manufacturer: 05/18/2016
• Supplement Date Received by Manufacturer: 05/18/2016
• Initial Report FDA Received Date: 08/10/2022
• Supplement Report FDA Received Date: 08/19/2022
• Was Device Evaluated by Manufacturer? (Y/N): Yes
• Date Device Manufactured: 01/14/2015
• 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
• Patient Sex: Unknown