MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2014-04-15 for MEDLINE URINAL DYND80235S manufactured by Medline Industries.
[4554678]
While using a plastic urinal, the penis was cut- skin laceration.
Patient Sequence No: 1, Text Type: D, B5
| Report Number | MW5035693 |
| MDR Report Key | 3759672 |
| Date Received | 2014-04-15 |
| Date of Report | 2014-04-14 |
| Date of Event | 2014-04-07 |
| Date Added to Maude | 2014-04-21 |
| 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 | OTHER HEALTH CARE PROFESSIONAL |
| 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 | MEDLINE URINAL |
| Generic Name | URINAL |
| Product Code | FNP |
| Date Received | 2014-04-15 |
| Catalog Number | DYND80235S |
| Operator | LAY USER/PATIENT |
| Device Availability | Y |
| Device Sequence No | 1 |
| Device Event Key | 0 |
| Manufacturer | MEDLINE INDUSTRIES |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 1. Other | 2014-04-15 |