TRILOGY 202 Adverse Event — Malfunction (MDR 2518422-2020-01076)
TRILOGY 202 Adverse Event — Malfunction (MDR 2518422-2020-01076) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: TRILOGY 202; Generic name: VENTILATOR, CONTINUOUS, FACILITY USE; Manufacturer: RESPIRONICS INC..
| Device | TRILOGY 202 |
|---|---|
| Generic name | VENTILATOR, CONTINUOUS, FACILITY USE |
| Manufacturer | RESPIRONICS INC. |
| Report number | 2518422-2020-01076 |
| Event type | Malfunction |
| Product problem | Y |
| Date received | 2020-04-27 |
| Report source | HEALTH PROFESSIONAL |
| Narrative | A VENTILATOR WAS RETURNED TO THE MANUFACTURER SERVICE. THERE WAS NO HARM OR INJURY REPORTED. DURING THE EVALUATION OF THE DEVICE AT THE MANUFACTURER'S SERVICE CENTER, "SERVICE REQUIRED" CODES WERE FOUND IN THE VENTILATOR'S DOWNLOADED ERROR LOG. THE DEVICE'S OXYGEN BLENDING MODULE BOARD WAS REPLACED TO ADDRESS THE ISSUES. |
| Source | openFDA MAUDE (device adverse events) |
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