BARDEX® LUBRI-SIL® I.C. ALL-SILICONE FOLEY CATHETER Adverse Event — Malfunction (MDR 1018233-2020-02904)
BARDEX® LUBRI-SIL® I.C. ALL-SILICONE FOLEY CATHETER Adverse Event — Malfunction (MDR 1018233-2020-02904) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: BARDEX® LUBRI-SIL® I.C. ALL-SILICONE FOLEY CATHETER; Generic name: FOLEY CATHETER (SILICONE); Manufacturer: C.R. BARD, INC. (C
| Device | BARDEX® LUBRI-SIL® I.C. ALL-SILICONE FOLEY CATHETER |
|---|---|
| Generic name | FOLEY CATHETER (SILICONE) |
| Manufacturer | C.R. BARD, INC. (COVINGTON) -1018233 |
| Report number | 1018233-2020-02904 |
| Event type | Malfunction |
| Product problem | Y |
| Date received | 2020-04-28 |
| Report source | DISTRIBUTOR, OTHER |
| Narrative | THE INVESTIGATION IS STILL IN PROGRESS. ONCE THE INVESTIGATION IS COMPLETE, A SUPPLEMENTAL REPORT WILL BE FILED. |
| Source | openFDA MAUDE (device adverse events) |
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