MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 1998-05-07 for DEVON 4810 * manufactured by Graphic Controls.
[96299]
Lid on sharps container will not stay sealed under normal handling conditions. No injury or exposures have occurred.
Patient Sequence No: 1, Text Type: D, B5
| Report Number | MW1013780 |
| MDR Report Key | 167543 |
| Date Received | 1998-05-07 |
| Date of Report | 1998-04-30 |
| Date of Event | 1998-04-22 |
| Date Added to Maude | 1998-05-18 |
| 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 | 0 |
| Reporter Occupation | RISK MANAGER |
| Health Professional | 3 |
| Initial Report to FDA | 0 |
| Report to FDA | 0 |
| Event Location | 3 |
| Single Use | 0 |
| Previous Use Code | 0 |
| Event Type | 3 |
| Type of Report | 3 |
| Brand Name | DEVON |
| Generic Name | 10 GALLON SHARPS CONTAINER/MAILBOX LID |
| Product Code | MML |
| Date Received | 1998-05-07 |
| Model Number | 4810 |
| Catalog Number | * |
| Lot Number | VARIOUS |
| ID Number | * |
| Operator | HEALTH PROFESSIONAL |
| Device Availability | Y |
| Implant Flag | N |
| Date Removed | * |
| Device Sequence No | 1 |
| Device Event Key | 163024 |
| Manufacturer | GRAPHIC CONTROLS |
| Manufacturer Address | 189 VAN RENSSELAER ST. BUFFALO NY 14240 US |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 1. Other | 1998-05-07 |