MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2015-06-02 for VRI manufactured by Medready.
[5940080]
Medication box does not rotate; top does not fit device correctly.
Patient Sequence No: 1, Text Type: D, B5
| Report Number | MW5043012 |
| MDR Report Key | 4834847 |
| Date Received | 2015-06-02 |
| Date of Report | 2015-06-02 |
| Date of Event | 2015-05-15 |
| Date Added to Maude | 2015-06-12 |
| 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 |
| 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 | VRI |
| Generic Name | ELECTRONIC MED BOX |
| Product Code | NXB |
| Date Received | 2015-06-02 |
| Device Sequence No | 1 |
| Device Event Key | 0 |
| Manufacturer | MEDREADY |
| Manufacturer Address | US |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 2015-06-02 |