MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2004-04-02 for CHARGING CABLE 2106 E60233-8 manufactured by Car-go-denver.
[28235747]
Respiratory failure while on a portable ventilator. A portable ventilator attached to a battery via a cable failed to operate.
Patient Sequence No: 1, Text Type: D, B5
| Report Number | 5145183 |
| MDR Report Key | 5145183 |
| Date Received | 2004-04-02 |
| Date of Report | 2004-03-31 |
| Date of Event | 2004-01-13 |
| Date Facility Aware | 2004-01-13 |
| Report Date | 2004-03-31 |
| Date Reported to FDA | 2004-03-31 |
| Date Added to Maude | 2015-10-13 |
| Event Key | 0 |
| Report Source Code | User Facility report |
| Manufacturer Link | N |
| Number of Patients in Event | 0 |
| Adverse Event Flag | 3 |
| Product Problem Flag | 3 |
| Reprocessed and Reused Flag | 3 |
| 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 | 0 |
| Brand Name | CHARGING CABLE |
| Generic Name | CABLE |
| Product Code | MOD |
| Date Received | 2004-04-02 |
| Model Number | 2106 |
| Catalog Number | E60233-8 |
| ID Number | 1320 |
| Device Availability | Y |
| Device Age | 6 MO |
| Device Eval'ed by Mfgr | I |
| Device Sequence No | 1 |
| Device Event Key | 0 |
| Manufacturer | CAR-GO-DENVER |
| Manufacturer Address | CO US |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 1. Life Threatening | 2004-04-02 |