SYNCHRON LX20 PRO Adverse Event — Malfunction (MDR 2050012-2008-00009)
SYNCHRON LX20 PRO Adverse Event — Malfunction (MDR 2050012-2008-00009) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: SYNCHRON LX20 PRO; Generic name: CLINICAL CHEMISTRY ANALYZER; Manufacturer: BECKMAN COULTER, INC..
| Device | SYNCHRON LX20 PRO |
|---|---|
| Generic name | CLINICAL CHEMISTRY ANALYZER |
| Manufacturer | BECKMAN COULTER, INC. |
| Report number | 2050012-2008-00009 |
| Event type | Malfunction |
| Product problem | Y |
| Date received | 2008-02-18 |
| Report source | Health Professional, HEALTH PROFESSIONAL |
| Source | openFDA MAUDE (device adverse events) |
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