CARESTATION 620 Adverse Event — Malfunction (MDR 9710602-2020-00143)
CARESTATION 620 Adverse Event — Malfunction (MDR 9710602-2020-00143) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: CARESTATION 620; Generic name: ANESTHESIA GAS MACHINE; Manufacturer: GE MEDICAL SYSTEMS (CHINA) CO., LTD (WUXI).
| Device | CARESTATION 620 |
|---|---|
| Generic name | ANESTHESIA GAS MACHINE |
| Manufacturer | GE MEDICAL SYSTEMS (CHINA) CO., LTD (WUXI) |
| Report number | 9710602-2020-00143 |
| Event type | Malfunction |
| Product problem | Y |
| Date received | 2020-04-27 |
| Report source | FOREIGN, HEALTH PROFESSIONAL, U |
| Narrative | A GE HEALTHCARE SERVICE REPRESENTATIVE PERFORMED A CHECKOUT OF THE SYSTEM AND CONFIRMED THE REPORTED ISSUE. THE POWER MANAGEMENT BOARD WAS REPLACED 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. UNIQUE IDENTIFIER: (B)(4). |
| Source | openFDA MAUDE (device adverse events) |
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