Device evidence

device-recall:cfres:118359

IDEV Technologies SUPERA VERITAS Interwoven Self-Expanding Nitinol Stent Transhepatic Biliary System. Indicated for palliative treatment of biliary strictures produced by malignant neoplasms

Official recall number

Z-1550-2013

Evidence summary

Product code: FGE
Recall status: Terminated
Event initiated: May 29, 2012
Root cause: Labeling mix-ups
Source snapshot: 5482458777762b1480c71ac49b2913b9c7984bb55aac66a4315d018da7cfed2c
Product: Z-1550-2013