CELL-DYN SAPPHIRE ANALYZER Adverse Event — Malfunction (MDR 2919069-2020-00013)
CELL-DYN SAPPHIRE ANALYZER Adverse Event — Malfunction (MDR 2919069-2020-00013) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: CELL-DYN SAPPHIRE ANALYZER; Generic name: AUTOMATED HEMATOLOGY ANALYZER; Manufacturer: ABBOTT DIAGNOSTICS DIVISION.
| Device | CELL-DYN SAPPHIRE ANALYZER |
|---|---|
| Generic name | AUTOMATED HEMATOLOGY ANALYZER |
| Manufacturer | ABBOTT DIAGNOSTICS DIVISION |
| Report number | 2919069-2020-00013 |
| Event type | Malfunction |
| Product problem | Y |
| Date received | 2020-04-28 |
| Report source | HEALTH PROFESSIONAL |
| Narrative | AN EVALUATION IS IN PROCESS. A FOLLOW-UP REPORT WILL BE SUBMITTED WHEN THE EVALUATION IS COMPLETE. |
| Source | openFDA MAUDE (device adverse events) |
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