ALIGN URETHRAL SUPPORT SYSTEM Adverse Event — Injury (MDR 1018233-2008-00007)
ALIGN URETHRAL SUPPORT SYSTEM Adverse Event — Injury (MDR 1018233-2008-00007) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: ALIGN URETHRAL SUPPORT SYSTEM; Manufacturer: C.R. BARD, INC.; Report number: 1018233-2008-00007.
| Device | ALIGN URETHRAL SUPPORT SYSTEM |
|---|---|
| Manufacturer | C.R. BARD, INC. |
| Report number | 1018233-2008-00007 |
| Event type | Injury |
| Product problem | N |
| Date received | 2008-02-19 |
| Report source | Company representation |
| Narrative | IT WAS REPORTED THAT IMMEDIATELY FOLLOWING A SLING PROCEDURE IN 2007, THE PATIENT WAS PLACED IN RETENTION. RETENTION WAS PROLONGED WITH SELF-CATHETERIZATION FOLLOWING A FOLEY CATHETER FOR 14 DAYS. THE DOCTOR PERFORMED A SLING LYSIS IN 2008. ADDITIONAL INFORMATION HAS BEEN REQUESTED BUT NOT YET RECEIVED. |
| Source | openFDA MAUDE (device adverse events) |
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