AESPIRE 7900 Adverse Event — Malfunction (MDR 2112667-2020-01347)
AESPIRE 7900 Adverse Event — Malfunction (MDR 2112667-2020-01347) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: AESPIRE 7900; Generic name: ANESTHESIA GAS MACHINE; Manufacturer: DATEX-OHMEDA, INC..
| Device | AESPIRE 7900 |
|---|---|
| Generic name | ANESTHESIA GAS MACHINE |
| Manufacturer | DATEX-OHMEDA, INC. |
| Report number | 2112667-2020-01347 |
| Event type | Malfunction |
| Product problem | Y |
| Date received | 2020-04-27 |
| Report source | HEALTH PROFESSIONAL, USER FACI |
| Narrative | CUSTOMER CONTACT REPORTS NO PATIENT INFORMATION AVAILABLE. A GE HEALTHCARE SERVICE REPRESENTATIVE PERFORMED A CHECKOUT OF THE SYSTEM, AND CONFIRMED THE REPORTED ISSUE. THE SENSOR INTERFACE BOARD (SIB) WAS REPLACED TO RESOLVE THE REPORTED ISSUE. |
| Source | openFDA MAUDE (device adverse events) |
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