MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2012-04-16 for BARD CUNNINGHAM CLAMP manufactured by Bard.
[2605601]
Seen by urologist for leaking and incontinence. Doctor recommended cunningham clamp put the clamp on the last notch, and was unable to release clamp. Had to bend the clamp up to release it. Now having pain and bleeding.
Patient Sequence No: 1, Text Type: D, B5
| Report Number | MW5025030 |
| MDR Report Key | 2537924 |
| Date Received | 2012-04-16 |
| Date of Report | 2012-04-16 |
| Date of Event | 2012-04-13 |
| Date Added to Maude | 2012-04-18 |
| Event Key | 0 |
| Report Source Code | Voluntary report |
| Manufacturer Link | N |
| Number of Patients in Event | 0 |
| Adverse Event Flag | 3 |
| Product Problem Flag | 3 |
| Reprocessed and Reused Flag | 3 |
| Reporter Occupation | PATIENT |
| Health Professional | 3 |
| Initial Report to FDA | 3 |
| Report to FDA | 0 |
| Event Location | 0 |
| Single Use | 0 |
| Previous Use Code | 0 |
| Event Type | 3 |
| Type of Report | 3 |
| Brand Name | BARD CUNNINGHAM CLAMP |
| Generic Name | CLAMP |
| Product Code | FHA |
| Date Received | 2012-04-16 |
| Device Availability | Y |
| Device Sequence No | 1 |
| Device Event Key | 0 |
| Manufacturer | BARD |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 2012-04-16 |