FDA Adverse Event
Malfunction
Summary report: N
COMPRESSOR MINI
MDR report key: 2223544
·
Received July 29, 2011
Report
- Report Number
- 8010042-2011-00128
- Event Type
- Malfunction
- Date Received
- July 29, 2011
- Date of Event
- June 5, 2011
- Report Date
- June 8, 2011
- Manufacturer
- MAQUET CRITICAL CARE AB
- Product Code
- BTI
- PMA / PMN Number
- K023354
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- TN, US
- Reporter Occupation
- OTHER
Narratives
Additional Manufacturer Narrative · 1
(B)(4).
Description of Event or Problem · 1
IT WAS REPORTED THAT THE POWER CORD ON COMPRESSOR SHOCKED A RESPIRATORY NURSE ON THE KNEE. IT WAS NOTICED THAT THE POWER CORD HAD FOUR BURN MARKS ON IT. (B)(4).
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | COMPRESSOR MINI | BTI | MAQUET CRITICAL CARE AB |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 |