MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2012-07-24 for COLOSTOMY DEVICES manufactured by .
[2736100]
Explain to me why i'm having so much trouble receiving a consistent supply of my colostomy devices. Incompetence and ineptness runs amok in america.
Patient Sequence No: 1, Text Type: D, B5
| Report Number | MW5026364 |
| MDR Report Key | 2682323 |
| Date Received | 2012-07-24 |
| Date Added to Maude | 2012-08-07 |
| 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 | 0 |
| 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 |
| Generic Name | COLOSTOMY DEVICES |
| Product Code | EZS |
| Date Received | 2012-07-24 |
| Device Sequence No | 1 |
| Device Event Key | 0 |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 2012-07-24 |