FDA Adverse Event
Injury
Summary report: N
2125050-2012-00001
MDR report key: 2402470
·
Received January 6, 2012
Report
- Report Number
- 2125050-2012-00001
- Event Type
- Injury
- Date Received
- January 6, 2012
- Manufacturer
- COLOPLAST MANUFACTURING US, LLC
- PMA / PMN Number
- K050148
- Adverse Event
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- US
- Reporter Occupation
- OTHER
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | NA | Female | Other |