ASTRAL 100 - EUR1 Adverse Event — Malfunction (MDR 3007573469-2020-00560)
ASTRAL 100 - EUR1 Adverse Event — Malfunction (MDR 3007573469-2020-00560) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: ASTRAL 100 - EUR1; Manufacturer: RESMED LTD; Report number: 3007573469-2020-00560.
| Device | ASTRAL 100 - EUR1 |
|---|---|
| Manufacturer | RESMED LTD |
| Report number | 3007573469-2020-00560 |
| Event type | Malfunction |
| Product problem | Y |
| Date received | 2020-04-28 |
| Narrative | IT WAS REPORTED TO RESMED THAT AN ASTRAL DEVICE FAILED TO COMPLETE ITS INTERNAL SELF-TEST. THERE WAS NO PATIENT HARM OR SERIOUS INJURY REPORTED AS A RESULT OF THIS INCIDENT. |
| Source | openFDA MAUDE (device adverse events) |
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