FDA Adverse Event
Injury
Summary report: N
JACKSON PRATT CARDIOTORACIC DRAIN
MDR report key: 5801815
·
Received July 18, 2016
Report
- Report Number
- 5801815
- Event Type
- Injury
- Date Received
- July 18, 2016
- Date of Event
- June 17, 2016
- Report Date
- July 6, 2016
- Manufacturer
- EVCO PLASTICS, DIV. DON EVANS, INC
- Product Code
- GCD
- Adverse Event
- Yes
- Report Source
- User Facility report
- Reporter Location
- CA, US
- Reporter Occupation
- NURSE
Narratives
Description of Event or Problem · 1
NURSE PRACTITIONER REMOVED JP DRAIN FROM PATIENT. SHE THEN ADVISED PRIMARY RN THAT PATIENT WOULD NEED STAT CT HEAD TO EVALUATE FOR POSSIBLE RETAINED DRAIN FRAGMENT. PATIENT TAKEN TO SURGERY AND DRAIN FRAGMENT WAS REMOVED. PATIENT CONDITION REMAINED SAME.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 455346 | JACKSON PRATT CARDIOTORACIC DRAIN | CONNECTOR, CATHETER | GCD | EVCO PLASTICS, DIV. DON EVANS, INC |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | 71 YR | Hospitalization| R |