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U.S. Department of Health and Human Services

MAUDE Adverse Event Report: RESPIRONICS, INC. BIPAP AUTO M SERIES; VENTILATOR, NON-CONTINUOUS (RESPIRATOR)

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RESPIRONICS, INC. BIPAP AUTO M SERIES; VENTILATOR, NON-CONTINUOUS (RESPIRATOR) Back to Search Results
Model Number IN701S
Device Problem Degraded (1153)
Patient Problem Pharyngitis (2367)
Event Date 02/01/2024
Event Type  malfunction  
Event Description
The manufacturer received information alleging dry throat.There is no allegation of serious or permanent harm or injury.No medical intervention was required by the patient.The manufacturer's investigation is ongoing.A follow-up report will be submitted when the manufacturer's investigation is complete.
 
Manufacturer Narrative
H3 other text : device not returned to manufacturer.
 
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Brand Name
BIPAP AUTO M 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 15208
4125423300
MDR Report Key18928832
MDR Text Key337983595
Report Number2518422-2024-14236
Device Sequence Number1
Product Code BZD
Combination Product (y/n)N
Reporter Country CodeHK
PMA/PMN Number
K061034
Number of Events Reported1
Summary Report (Y/N)N
Report Source Manufacturer
Source Type Consumer
Reporter Occupation Non-Healthcare Professional
Remedial Action Recall
Type of Report Initial
1 Device was Involved in the Event
1 Patient was Involved in the Event
Date FDA Received03/19/2024
Is this an Adverse Event Report? No
Is this a Product Problem Report? Yes
Device Operator Lay User/Patient
Device Model NumberIN701S
Device Catalogue NumberIN701S
Was Device Available for Evaluation? No
Date Manufacturer Received02/01/2024
Was Device Evaluated by Manufacturer? No
Date Device Manufactured11/05/2007
Is the Device Single Use? No
Is This a Reprocessed and Reused Single-Use Device? No
Removal/Correction NumberZ-1974-2021
Patient Sequence Number1
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