MAGIC3¿ INTERMITTENT CATHETER WITH SURE-GRIP¿ SLEEVE Adverse Event — Malfunction (MDR 1018233-2020-02902)
MAGIC3¿ INTERMITTENT CATHETER WITH SURE-GRIP¿ SLEEVE Adverse Event — Malfunction (MDR 1018233-2020-02902) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: MAGIC3¿ INTERMITTENT CATHETER WITH SURE-GRIP¿ SLEEVE; Generic name: MAGIC 3 CATHETER; Manufacturer: C.R. BARD, INC. (COVINGTO
| Device | MAGIC3¿ INTERMITTENT CATHETER WITH SURE-GRIP¿ SLEEVE |
|---|---|
| Generic name | MAGIC 3 CATHETER |
| Manufacturer | C.R. BARD, INC. (COVINGTON) -1018233 |
| Report number | 1018233-2020-02902 |
| Event type | Malfunction |
| Product problem | Y |
| Date received | 2020-04-28 |
| Report source | CONSUMER, OTHER |
| Narrative | THE REPORTED EVENT COULD NOT BE CONFIRMED. IT WAS UNKNOWN WHETHER THE DEVICE MET SPECIFICATIONS SINCE THE SAMPLE WAS NOT RETURNED FOR EVALUATION. THE PRODUCT WAS USED FOR TREATMENT PURPOSES. A POTENTIAL FAILURE MODE COULD BE ¿VISCOSITY TOO HIGH/LOW¿ WITH A POTENTIAL ROOT CAUSE OF ¿OPERATOR ERROR OR MECHANICAL FAILURE¿. THE LOT NUMBER IS UNKNOWN THEREFORE THE DEVICE HISTORY RECORD COULD NOT BE REVI |
| Source | openFDA MAUDE (device adverse events) |
🔍 Search all device adverse events →
$1999/mo
Try DeviceEvents →