FDA Adverse Event
Injury
Summary report: N
HUMMINGBIRD VENTRICULAR
MDR report key: 5048851
·
Received August 12, 2015
Report
- Report Number
- 5048851
- Event Type
- Injury
- Date Received
- August 12, 2015
- Date of Event
- August 1, 2015
- Report Date
- August 11, 2015
- Manufacturer
- INNERSPACE INC.
- Product Code
- HCA
- Product Problem
- Yes
- Report Source
- User Facility report
- Reporter Location
- HI, US
- Reporter Occupation
- OTHER HEALTH CARE PROFESSIONAL
Narratives
Description of Event or Problem · 1
DURING PLACEMENT OF THE VENTRICULOSTOMY CATHETER THE FIRST CATHETER INSERTED UNFORTUNATELY WAS FRACTURED OR LACERATED BY THE INNER TABLE AND A FRAGMENT OF CATHETER WAS LEFT IN SITU.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 532302 | HUMMINGBIRD VENTRICULAR | VENTRICULAR CATHETER | HCA | INNERSPACE INC. | H200MR | 140616-03 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | 24 YR | Hospitalization |