FDA Adverse Event
Malfunction
Summary report: N
1226348-2013-20004
MDR report key: 2953801
·
Received February 9, 2013
Report
- Report Number
- 1226348-2013-20004
- Event Type
- Malfunction
- Date Received
- February 9, 2013
- Date of Event
- January 15, 2013
- Report Date
- January 18, 2013
- PMA / PMN Number
- K072173
- Adverse Event
- Yes
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Occupation
- HEALTH PROFESSIONAL