FDA Adverse Event
Malfunction
Summary report: N
GUARDIAN II NC HEMOSTASIS VALVE
MDR report key: 2994429
·
Received March 8, 2013
Report
- Report Number
- 3005395947-2013-00006
- Event Type
- Malfunction
- Date Received
- March 8, 2013
- Date of Event
- January 4, 2013
- Report Date
- March 8, 2013
- Manufacturer
- VASCULAR SOLUTIONS ZERUSA LIMITED
- Product Code
- DTL
- PMA / PMN Number
- K122301
- Removal / Correction Number
- 3005395947-02/28/2013-01
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- MO, US
- Reporter Occupation
- PHYSICIAN
Narratives
Description of Event or Problem · 1
USER-FACILITY REPORTED PHYSICIANS EXPERIENCING INTRODUCTION OF AIR WHILE USING THE GUARDIAN II NC HEMOSTASIS VALVE.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 99715 | GUARDIAN II NC HEMOSTASIS VALVE | HEMOSTASIS VALVE | DTL | VASCULAR SOLUTIONS ZERUSA LIMITED | 8216 | 25615 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | Life Threatening |