COAGUCHEK SOFTCLIX Adverse Event — Malfunction (MDR 1823260-2020-01129)
COAGUCHEK SOFTCLIX Adverse Event — Malfunction (MDR 1823260-2020-01129) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: COAGUCHEK SOFTCLIX; Generic name: BLOOD LANCET; Manufacturer: ROCHE DIAGNOSTICS.
| Device | COAGUCHEK SOFTCLIX |
|---|---|
| Generic name | BLOOD LANCET |
| Manufacturer | ROCHE DIAGNOSTICS |
| Report number | 1823260-2020-01129 |
| Event type | Malfunction |
| Product problem | Y |
| Date received | 2020-04-28 |
| Report source | CONSUMER |
| Narrative | OCCUPATION - THE OCCUPATION IS LAY USER/PATIENT. THE YEAR IS THE ONLY KNOWN PART OF MANUFACTURE DATE. WE HAVE DEFAULTED TO THE FIRST OF THE YEAR. THE CUSTOMER¿S PRODUCT HAS BEEN REQUESTED FOR RETURN. THE PRODUCT HAS NOT BEEN RECEIVED AT THIS TIME. IF THE PRODUCT IS RETURNED IN THE FUTURE, A FOLLOW UP REPORT WILL BE SUBMITTED. |
| Source | openFDA MAUDE (device adverse events) |
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