MAUDE Adverse Event Report: RESPIRONICS, INC. BIPAP S/T C SERIES; VENTILATOR, NON-CONTINUOUS (RESPIRATOR)

Model Number IN1061X

Device Problem Degraded (1153)

Patient Problems Headache (1880); Dizziness (2194); Respiratory Tract Infection (2420); Eye Infections (4466); Swelling/ Edema (4577)

Event Date 01/05/2022

Event Type  malfunction  

Event Description

The manufacturer was contacted in reference to the voluntary field safety notice / recall notification related to the sound abatement foam in certain cpap, bipap, and mechanical ventilator devices.The manufacturer received information alleging an issue related to a bipap device's sound abatement foam.The patient has alleged to experiencing eye and respiratory tract infections, headaches, dizziness and swollen cheekbones.There was no report of serious patient harm or injury.There was no medical intervention required by the patient.The manufacturer's investigation is ongoing.A follow-up report will be submitted when the manufacturer's investigation is complete.

• Brand Name: BIPAP S/T C SERIES
• Type of Device: 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: 15412564
• MDR Text Key: 303815971
• Report Number: 2518422-2022-80718
• Device Sequence Number: 1
• Product Code: MNS
• UDI-Device Identifier: 00606959039100
• UDI-Public: 00606959039100
• Combination Product (y/n): N
• Reporter Country Code: SP
• PMA/PMN Number: K102465
• Number of Events Reported: 1
• Summary Report (Y/N): N
• Report Source: Manufacturer
• Source Type: Foreign,Consumer,Company Representative,Distributor
• Reporter Occupation: Other
• Remedial Action: Recall
• Type of Report: Initial
• Report Date: 09/13/2022

1 Device was Involved in the Event

1 Patient was Involved in the Event

• Date FDA Received: 09/13/2022
• Is this an Adverse Event Report?: No
• Is this a Product Problem Report?: Yes
• Device Operator: Lay User/Patient
• Device Model Number: IN1061X
• Device Catalogue Number: IN1061X
• Was Device Available for Evaluation?: No
• Date Manufacturer Received: 01/10/2022
• Was Device Evaluated by Manufacturer?: No
• Date Device Manufactured: 10/02/2013
• Is the Device Single Use?: No
• Is This a Reprocessed and Reused Single-Use Device?: No
• Type of Device Usage: Unknown
• Removal/Correction Number: RES 88058
• Patient Sequence Number: 1