FDA Adverse Event
Death
Summary report: N
DLP PERFUSION ADAPTOR
MDR report key: 1634848
·
Received March 16, 2010
Report
- Report Number
- 1634848
- Event Type
- Death
- Date Received
- March 16, 2010
- Date of Event
- December 24, 2009
- Report Date
- March 16, 2010
- Manufacturer
- MEDTRONIC
- Product Code
- DTL
- Adverse Event
- Yes
- Report Source
- User Facility report
- Reporter Location
- IL, US
- Reporter Occupation
- RISK MANAGER
Narratives
Description of Event or Problem · 1
WHILE MOVING PATIENT FOR BASIC NURSING CARE, ADAPTOR SNAPPED. PATIENT STARTED TO BLEED FROM CATHETERS AS A RESULT.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | DLP PERFUSION ADAPTOR | ADAPTOR, CARDIOPULMONARY BYPASS | DTL | MEDTRONIC | * | UNK |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | 39 YR | Death | CARDIAC DRUGS| LONG-TERM ANTIBIOTICS |