MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2016-01-26 for CAPNOSTREAM 20 CAPOSTREAM 20 manufactured by Medtronic.
[37032364]
Medtronic / covidien / oridion capnography co2 monitor caught on fire sitting in a bay while charging the battery. The fire department was called and extinguished the fire.
Patient Sequence No: 1, Text Type: D, B5
| Report Number | MW5059708 |
| MDR Report Key | 5396670 |
| Date Received | 2016-01-26 |
| Date of Report | 2016-01-26 |
| Date of Event | 2016-01-26 |
| Date Added to Maude | 2016-01-28 |
| Event Key | 0 |
| Report Source Code | Voluntary report |
| Manufacturer Link | N |
| Number of Patients in Event | 0 |
| Adverse Event Flag | 3 |
| Product Problem Flag | 3 |
| Reprocessed and Reused Flag | 3 |
| Reporter Occupation | OTHER HEALTH CARE PROFESSIONAL |
| Health Professional | 3 |
| Initial Report to FDA | 3 |
| Report to FDA | 3 |
| Event Location | 3 |
| Single Use | 3 |
| Previous Use Code | 3 |
| Event Type | 3 |
| Type of Report | 3 |
| Brand Name | CAPNOSTREAM 20 |
| Generic Name | CO2 MONITOR |
| Product Code | LKD |
| Date Received | 2016-01-26 |
| Model Number | CAPOSTREAM 20 |
| ID Number | 173570 |
| Operator | HEALTH PROFESSIONAL |
| Device Availability | * |
| Device Eval'ed by Mfgr | * |
| Device Sequence No | 1 |
| Device Event Key | 0 |
| Manufacturer | MEDTRONIC |
| Manufacturer Address | MINNEAPOLIS MN 55432 US 55432 |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 1. Other | 2016-01-26 |