IDEV Technologies, Inc. recalls IDEV Technologies SUPERA VERITAS Interwoven Self-Expanding Nitinol Stent Transhepatic Biliary System. Indicated for pall

Recalled June 26, 2013 · FDA recall Z-1550-2013 · IDEV Technologies

Hazard

There was an error on the outer labeling of this device. The inner label was correct. · FDA Class II

Units

Sold at

Nationwide Distribution to the states of FL, NY, and PA.

Description

There was an error on the outer labeling of this device. The inner label was correct.

Product

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

Manufacturer(s)

IDEV Technologies, Inc.

Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →