AISYS Adverse Event — Malfunction (MDR 2112667-2020-01348)
AISYS Adverse Event — Malfunction (MDR 2112667-2020-01348) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: AISYS; Generic name: ANESTHESIA GAS MACHINE; Manufacturer: DATEX-OHMEDA, INC..
| Device | AISYS |
|---|---|
| Generic name | ANESTHESIA GAS MACHINE |
| Manufacturer | DATEX-OHMEDA, INC. |
| Report number | 2112667-2020-01348 |
| Event type | Malfunction |
| Product problem | Y |
| Date received | 2020-04-27 |
| Report source | DISTRIBUTOR, FOREIGN, HEALTH PR |
| Narrative | THE DISTRIBUTOR PERFORMED A CHECKOUT OF THE EQUIPMENT AND CONFIRMED THE REPORTED COMPLAINT. THE ANESTHESIA CONTROL BOARD (ACB) CABLE WAS REST TO RESOLVE THE REPORTED ISSUE. NO REPORT OF PATIENT INVOLVEMENT. THE INITIAL REPORTER IS LOCATED OUTSIDE THE U.S., AND THEREFORE THIS INFORMATION IS NOT PROVIDED DUE TO COUNTRY PRIVACY LAWS. |
| Source | openFDA MAUDE (device adverse events) |
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