FDA Adverse Event
Summary report: N
CONSTAVAC
MDR report key: 1913120
·
Received November 15, 2010
Report
- Report Number
- 1913120
- Date Received
- November 15, 2010
- Date of Event
- November 2, 2010
- Report Date
- November 15, 2010
- Manufacturer
- STRYKER
- Product Code
- GCY
- Report Source
- User Facility report
- Reporter Location
- NH, US
Narratives
Description of Event or Problem · 1
CONSTVAC WOULD NOT MAINTAIN THE APPRPRIATE SUCTION AND REQUIRED THE EXCHANGE OF A CONTAINER DURING THE PATIENT'S RECOVERY PERIOD.====================== HEALTH PROFESSIONAL'S IMPRESSION======================STAFF ARE SUSPECTING REPEAT BATTERY FAILURE.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | CONSTAVAC | CONSTAVAC | GCY | STRYKER | STRYKER #225-414S2 | 10209012 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | * |