MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2017-08-08 for MOBILE COMPUTER CART manufactured by Unk.
[82565713]
Battery/inverter unit for mobile medical computer cart plugged in to wall outlet began to smoke heavily during episode of pt care. Therapy duration: 1 year. Diagnosis or reason for use: electronic documentation. Event abated after use stopped or dose reduced: yes.
Patient Sequence No: 1, Text Type: D, B5
| Report Number | MW5071489 |
| MDR Report Key | 6785200 |
| Date Received | 2017-08-08 |
| Date of Report | 2017-08-08 |
| Date of Event | 2017-07-21 |
| Date Added to Maude | 2017-08-10 |
| 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 | 0 |
| Brand Name | MOBILE COMPUTER CART |
| Generic Name | MEDICAL COMPUTERS AND SOFTWARE |
| Product Code | LNX |
| Date Received | 2017-08-08 |
| Device Availability | Y |
| Device Eval'ed by Mfgr | I |
| Device Sequence No | 1 |
| Device Event Key | 0 |
| Manufacturer | UNK |
| Manufacturer Address | UNK UNK |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 1. Other | 2017-08-08 |