FDA Adverse Event
Injury
Summary report: N
CBC II CONSTAVAC
MDR report key: 581630
·
Received March 9, 2005
Report
- Report Number
- MW1034893
- Event Type
- Injury
- Date Received
- March 9, 2005
- Date of Event
- January 11, 2005
- Report Date
- March 9, 2005
- Manufacturer
- STRYKER INSTRUMENTS
- Product Code
- CAC
- Product Problem
- Yes
- Report Source
- Voluntary report
- Reporter Location
- MN, US
- Reporter Occupation
- OTHER
Narratives
Description of Event or Problem · 1
UNABLE TO GET CONSTAVAC DRAIN TO DRAIN BLOOD TO AUTOTRANSFUSE-THERE WAS 400 CC. PT UNABLE TO GET OWN BLOOD BACK.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | CBC II CONSTAVAC | AUTOTRANSFUSER | CAC | STRYKER INSTRUMENTS | CBC II CONSTAVAC | 04314BG2 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | 69 YR | Required Intervention |