BIPAP A30
Report
- Report Number
- 2518422-2022-10235
- Event Type
- Malfunction
- Date Received
- March 20, 2022
- Date of Event
- December 10, 2013
- Report Date
- April 18, 2022
- Manufacturer
- RESPIRONICS, INC.
- Product Code
- MNS
- PMA / PMN Number
- K113053
- Removal / Correction Number
- RES 88058
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- FR
- Reporter Occupation
- 003
Narratives
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.
THE MANUFACTURER PREVIOUSLY REPORTED THAT HOSPITALIZATION. INITIAL OR PROLONGED, 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, COMMON DEVICE NAME AND RAND NAME ARE UPDATED.
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 |
|---|---|---|---|---|---|---|---|
| 1974417 | BIPAP A30 | VENTILATOR, CONTINUOUS, NON-LIFE-SUPPORTING | MNS | RESPIRONICS, INC. | 951P | ||
| 629259 | BIPAP A30 | VENTILATOR, CONTINUOUS, NON-LIFE-SUPPORTING | MNS | RESPIRONICS, INC. | 951P |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | Unknown | Hospitalization| R |