MalfunctionOKC
SECURACATH
Received Apr 12, 2019 · Event occurred Mar 28, 2019
Report 8508593 · MDR key 8508593
Device
Generic name
Implanted Subcutaneous Securement Catheter
Manufacturer
Interrad Medical, IncModel number
7FCatalog number
400120
Lot number
A1850
Product problems
- Obstruction of Flow
Patient
Not reported
- No Known Impact Or Consequence To Patient
- No Known Impact Or Consequence To Patient
Narrative
Description of Event or Problem
AFTER INSERTING A DOUBLE LUMEN CENTRAL VENOUS LINE, MD APPLIED 7 FR SECURE-A-CATH AND NOTED THAT THE LINES WERE OCCLUDED FOLLOWING APPLICATION OF THE DEVICE. DEVICE REMOVED.