FDA Adverse Event Injury Summary report: N

SUPERDIMENSION BRONCHUS SYSTEM (SDBS)

MDR report key: 1598435 · Received January 28, 2010

Report

Report Number
3004659744-2010-00003
Event Type
Injury
Date Received
January 28, 2010
Date of Event
December 8, 2009
Report Date
January 28, 2010
Manufacturer
SUPERDIMENSION, LTD.
Product Code
JAK
PMA / PMN Number
K042438
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
GA, US
Reporter Occupation
PHYSICIAN

Narratives

Additional Manufacturer Narrative · 1

PNEUMOTHORAX IS A KNOWN COMPLICATION WHEN A LUNG BIOPSY IS PERFORMED DURING A TRANSBRONCHIAL LUNG BIOPSY, OR CT-GUIDED PERCUTANEOUS BIOPSY WITH COMPLICATION RATES UP TO APPROX 27% WITH THE CT GUIDED PROCEDURE. BIOPSY TOOLS ARE DESIGNED TO HAVE SHARP EDGES AND THEIR FUNCTION IS TO PUNCTURE OR OTHERWISE PENETRATE THE TISSUE IN ORDER TO COLLECT A SPECIMEN.

Description of Event or Problem · 1

THE SITE REPORTED (ON (B) (6) 2010) THAT THEY HAD A SUPERDIMENSION CASE ABOUT A MONTH AGO IN WHICH THE PT DEVELOPED A SLIGHT PNEUMOTHORAX. IT WAS REPORTED THAT A CHEST TUBE WAS PLACED AND THE NEXT DAY, THE PT WAS RELEASED FROM THE HOSPITAL. THERE WAS NO ALLEGATION THAT THE SUPERDIMENSION SYSTEM CAUSED THE REPORTED PNEUMOTHORAX.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 SUPERDIMENSION BRONCHUS SYSTEM (SDBS) COMPUTED TOMOGRAPHY X-RAY SYSTEM JAK SUPERDIMENSION, LTD.

Patients

Seq Age Sex Outcome Treatment
1 Hospitalization