INX FOR INLINE Adverse Event — Malfunction (MDR 1523574-2020-00010)
INX FOR INLINE Adverse Event — Malfunction (MDR 1523574-2020-00010) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: INX FOR INLINE; Generic name: INX FOR INLINE; Manufacturer: FERNO-WASHINGTON, INC..
| Device | INX FOR INLINE |
|---|---|
| Generic name | INX FOR INLINE |
| Manufacturer | FERNO-WASHINGTON, INC. |
| Report number | 1523574-2020-00010 |
| Event type | Malfunction |
| Product problem | N |
| Date received | 2020-04-27 |
| Report source | OTHER |
| Narrative | IT WAS REPORTED WHILE ON A CALL THE LEGS OF THE STRETCHER WOULD ALLEGEDLY NOT OPERATE USING POWER. THE MANUAL RELEASE WAS CONFIRMED TO BE OPERATIONAL; HOWEVER, THE MEDICS CALLED A 2ND TRUCK TO CONTINUE THE PATIENT TRANSPORT ON ANOTHER STRETCHER. NO INJURY OR ADVERSE EFFECT WAS REPORTED AS A RESULT. |
| Source | openFDA MAUDE (device adverse events) |
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