FDA Adverse Event
Injury
Summary report: N
SUPERDIMENSION INREACH BRONCHUS SYSTEM
MDR report key: 4919415
·
Received July 16, 2015
Report
- Report Number
- 3004962788-2015-00047
- Event Type
- Injury
- Date Received
- July 16, 2015
- Date of Event
- June 19, 2015
- Report Date
- July 16, 2015
- Manufacturer
- SUPERDIMENSION INC.
- Product Code
- JAK
- PMA / PMN Number
- K092365
- Adverse Event
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- WV, US
- Reporter Occupation
- PHYSICIAN
Narratives
Additional Manufacturer Narrative · 1
SUPERDIMENSION HAS REQUESTED THE DEVICE FOR EVALUATION BUT HAS NOT RECEIVED ANYTHING TO DATE. THERE WERE NO ANOMALIES IDENTIFIED DURING THE INTERNAL REVIEW OF THE DHR OF THE SYSTEM CONSOLE. PNEUMOTHORAX IS A KNOWN SHORT TERM COMPLICATION WHEN A LUNG BIOPSY IS PERFORMED DURING A TRANSBRONCHIAL LUNG BIOPSY OR CT GUIDED PERCUTANEOUS BIOPSY. IF ADDITIONAL INFORMATION IS RECEIVED A FOLLOW-UP REPORT WILL BE SUBMITTED.
Description of Event or Problem · 1
THE PATIENT SUFFERED A PNEUMOTHORAX DURING A SUPERDIMENSION PROCEDURE. THE PATIENT WAS HOSPITALIZED AND RELEASED. IF ADDITIONAL INFORMATION PERTINENT TO THE INCIDENT IS OBTAINED A FOLLOW-UP REPORT WILL BE SUBMITTED.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 462572 | SUPERDIMENSION INREACH BRONCHUS SYSTEM | ELECTROMAGNETIC NAVIGATION BRONCHOSCOPY | JAK | SUPERDIMENSION INC. | AAS00161-20 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | Hospitalization| O |