BARDIA® COUDE OLIVE TIP URETHRAL FOLEY CATHETER Adverse Event — Malfunction (MDR 1018233-2020-02829)
BARDIA® COUDE OLIVE TIP URETHRAL FOLEY CATHETER Adverse Event — Malfunction (MDR 1018233-2020-02829) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: BARDIA® COUDE OLIVE TIP URETHRAL FOLEY CATHETER; Generic name: COUDE INTERMITTENT CATHETER; Manufacturer: C.R. BARD, INC. (COVINGT
| Device | BARDIA® COUDE OLIVE TIP URETHRAL FOLEY CATHETER |
|---|---|
| Generic name | COUDE INTERMITTENT CATHETER |
| Manufacturer | C.R. BARD, INC. (COVINGTON) -1018233 |
| Report number | 1018233-2020-02829 |
| Event type | Malfunction |
| Product problem | Y |
| Date received | 2020-04-27 |
| Report source | CONSUMER, DISTRIBUTOR, OTHER |
| Narrative | IT WAS REPORTED THAT SOME OF THE CATHETERS WERE BENT IN THE PACKAGING. |
| Source | openFDA MAUDE (device adverse events) |
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