FDA Adverse Event
Death
Summary report: N
PRESSURE INFUSION BAGS
MDR report key: 1578953
·
Received January 13, 2010
Report
- Report Number
- 1721504-2010-00010
- Event Type
- Death
- Date Received
- January 13, 2010
- Report Date
- December 14, 2009
- Manufacturer
- MERIT MEDICAL SYSTEMS, INC.
- Product Code
- KZD
- PMA / PMN Number
- EXEMPT
- Adverse Event
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- OR, US
- Reporter Occupation
- NOT APPLICABLE
Narratives
Additional Manufacturer Narrative · 1
DEVICE EVAL - DEVICE IN QUESTION HAS NOT BEEN RETURNED FOR EVAL. CONCLUSION - A FOLLOW-UP REPORT WILL BE SUBMITTED IF ADD'L INFO IS REC'D.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | PRESSURE INFUSION BAGS | INFUSOR, PRESSURE, FOR IV BAGS | KZD | MERIT MEDICAL SYSTEMS, INC. |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 |