MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2013-12-31 for AIR HANDLERS manufactured by .
[3990101]
In cvdr, air handlers are down, temp in room is 72 and no negative pressure in room.
Patient Sequence No: 1, Text Type: D, B5
| Report Number | MW5034499 |
| MDR Report Key | 3632229 |
| Date Received | 2013-12-31 |
| Date of Report | 2013-12-27 |
| Date of Event | 2013-08-12 |
| Date Added to Maude | 2014-02-20 |
| 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 | NA |
| Generic Name | AIR HANDLERS |
| Product Code | FRF |
| Date Received | 2013-12-31 |
| Operator | OTHER |
| Device Availability | N |
| Device Sequence No | 1 |
| Device Event Key | 0 |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 2013-12-31 |