FDA Adverse Event Malfunction Summary report: N

BIPAP ST

MDR report key: 13831311 · Received March 20, 2022

Report

Report Number
2518422-2022-10225
Event Type
Malfunction
Date Received
March 20, 2022
Date of Event
November 13, 2013
Report Date
April 18, 2022
Manufacturer
RESPIRONICS, INC.
Product Code
MNS
PMA / PMN Number
K102465
Removal / Correction Number
RES 88058
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
FR
Reporter Occupation
003

Narratives

Additional Manufacturer Narrative · 0

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.

Additional Manufacturer Narrative · 0

THE MANUFACTURER PREVIOUSLY REPORTED THAT REQUIRED INTERVENTION TO PREVENT PERMANENT IMPAIRMENT/DAMAGE, OCCURED. AFTER REVIEW, IT WAS DETERMINED THAT THIS OPTIONS WERE INCORRECTLY SELECTED. NOTHING SUCH HAS OCCURED TO THE PATIENT. THE REPORT SHOULD HAVE BEEN SENT FOR PRODUCT PROBLEM ONLY. TYPE OF INVESTIGATION CODE WAS MISSING. THE MISSING VALUE IS 10. PMA/510(K) NUMBER WAS INCORRECT THE CORRECT VALUE IS K102465. INITIAL REPORTER, DEVICE EVALUATED BY MANUFACTURER, AND COMMON DEVICE NAME ARE UPDATED.

Description of Event or Problem · 0

THE MANUFACTURER RECEIVED INFORMATION ALLEGING AN ISSUE RELATED TO A 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.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1974416 BIPAP ST VENTILATOR, CONTINUOUS, NON-LIFE-SUPPORTING MNS RESPIRONICS, INC. 1061402
541360 BIPAP ST VENTILATOR, CONTINUOUS, NON-LIFE-SUPPORTING MNS RESPIRONICS, INC. 1061402

Patients

Seq Age Sex Outcome Treatment
1 Unknown Required Intervention