BARD® INLAY® URETERAL STENT WITH HYDROGLIDE¿ GUIDEWIRE Adverse Event — Malfunction (MDR 1018233-2020-02850)
BARD® INLAY® URETERAL STENT WITH HYDROGLIDE¿ GUIDEWIRE Adverse Event — Malfunction (MDR 1018233-2020-02850) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: BARD® INLAY® URETERAL STENT WITH HYDROGLIDE¿ GUIDEWIRE; Generic name: URETERAL STENT; Manufacturer: C.R. BARD, INC. (COVING
| Device | BARD® INLAY® URETERAL STENT WITH HYDROGLIDE¿ GUIDEWIRE |
|---|---|
| Generic name | URETERAL STENT |
| Manufacturer | C.R. BARD, INC. (COVINGTON) -1018233 |
| Report number | 1018233-2020-02850 |
| Event type | Malfunction |
| Product problem | Y |
| Date received | 2020-04-27 |
| Report source | COMPANY REPRESENTATIVE, HEALTH |
| Narrative | THE INVESTIGATION IS STILL IN PROGRESS. ONCE THE INVESTIGATION IS COMPLETE A SUPPLEMENTAL REPORT WILL BE FILED. THE DEVICE WAS NOT RETURNED. |
| Source | openFDA MAUDE (device adverse events) |
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