BARD® URETHRAL CATHETER Adverse Event — Malfunction (MDR 1018233-2020-02864)
BARD® URETHRAL CATHETER Adverse Event — Malfunction (MDR 1018233-2020-02864) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: BARD® URETHRAL CATHETER; Generic name: 2 EYE TIEMAAN CATHETER; Manufacturer: C.R. BARD, INC. (COVINGTON) -1018233.
| Device | BARD® URETHRAL CATHETER |
|---|---|
| Generic name | 2 EYE TIEMAAN CATHETER |
| Manufacturer | C.R. BARD, INC. (COVINGTON) -1018233 |
| Report number | 1018233-2020-02864 |
| Event type | Malfunction |
| Product problem | Y |
| Date received | 2020-04-27 |
| Report source | CONSUMER, OTHER |
| Narrative | THE REPORTED EVENT WAS CONFIRMED AS USE-RELATED. NO SAMPLE WAS RETURNED. ACCORDING TO THE EVENT "THE LAST BATCH OF CATHETERS HE RECEIVED HAVE BEEN CLOGGING UP WITH THE SURGILUBE HE USES TO LUBRICATE THE CATHETERS." AS THE EVENT STATED THAT BLOCKAGE WAS CLEARED AFTER USING WATER TO THIN THE LUBRICANT AND QUALITY CONFIRMED THAT THE CATHETER IS INTENDED FOR USE WITHOUT LUBRICANT, THE REPORTED EVENT W |
| Source | openFDA MAUDE (device adverse events) |
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