FDA Adverse Event
Malfunction
Summary report: N
9680353-2011-00066
MDR report key: 2883685
·
Received December 21, 2012
Report
- Report Number
- 9680353-2011-00066
- Event Type
- Malfunction
- Date Received
- December 21, 2012
- Report Date
- March 23, 2026
- Manufacturer
- CORPORATION STERIS CANADA
- Report Source
- Manufacturer report
- Reporter Occupation
- OTHER
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | NA | Unknown |