FDA Adverse Event
Malfunction
Summary report: N
IMPACT 73X PORTABLE VENTILATOR SYSTEM
MDR report key: 4178523
·
Received October 16, 2014
Report
- Report Number
- 2242630-2014-00001
- Event Type
- Malfunction
- Date Received
- October 16, 2014
- Date of Event
- May 29, 2014
- Report Date
- July 30, 2014
- Manufacturer
- IMPACT INSTRUMENTATION, INC.
- Product Code
- BTL
- PMA / PMN Number
- K051476
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- CA, US
- Reporter Occupation
- OTHER HEALTH CARE PROFESSIONAL
Narratives
Description of Event or Problem · 1
(B)(4) THIS SYSTEM WAS RETURNED TO THE MANUFACTURE FOR NORMAL PREVENTATIVE MAINTENANCE. IT WAS DETERMINED THAT THE ALARM, AUDIBLE TYPE, WAS INTERMITTENT AND NEEDED TO BE REPLACED.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 659637 | IMPACT 73X PORTABLE VENTILATOR SYSTEM | VENTILATOR | BTL | IMPACT INSTRUMENTATION, INC. | 73X | NA |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | NONE REPORTED BY THE OPERATOR |