TBD Adverse Event — Malfunction (MDR 1523574-2020-00011)
TBD Adverse Event — Malfunction (MDR 1523574-2020-00011) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: TBD; Generic name: TBD; Manufacturer: FERNO-WASHINGTON, INC..
| Device | TBD |
|---|---|
| Generic name | TBD |
| Manufacturer | FERNO-WASHINGTON, INC. |
| Report number | 1523574-2020-00011 |
| Event type | Malfunction |
| Product problem | N |
| Date received | 2020-04-27 |
| Report source | OTHER |
| Narrative | IT WAS REPORTED WHILE TRANSPORTING A STRETCHER IN THE BACK OF THE AMBULANCE THE STRETCHER CAME LOOSE FROM THE FASTENER. THERE WAS NO PATIENT ON THE STRETCHER AT THE TIME OF INCIDENT AND THERE HAVE BEEN NO ALLEGATIONS OF INJURY AS A RESULT OF THE INCIDENT. THE COMPLAINANT HAS NOT ALLEGED A MALFUNCTION OF THE STRETCHER AND THE FASTENER IS STILL IN SERVICE; HOWEVER, THEY ARE MANUALLY ENGAGING THE FAS |
| Source | openFDA MAUDE (device adverse events) |
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