FDA Adverse Event
Malfunction
Summary report: N
3007305485-2011-00003
MDR report key: 1974678
·
Received January 31, 2011
Report
- Report Number
- 3007305485-2011-00003
- Event Type
- Malfunction
- Date Received
- January 31, 2011
- Date of Event
- December 20, 2010
- Report Date
- March 17, 2011
- Manufacturer
- CONSOLIDATED MEDICAL EQUIPMENT COMPANY
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- IL, US
- Reporter Occupation
- OTHER
- Health Professional
- *
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | NA | Unknown |