IDEV Technologies, Inc.: Medical Device Recall in 2013 - (Recall #: Z-1550-2013)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2013.

Data Source: FDA.

Product Description:

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

Product Classification:

Class II

Date Initiated: May 29, 2012

Date Posted: June 26, 2013

Recall Number: Z-1550-2013

Event ID: 65245

Reason for Recall:

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

Status: Terminated

Product Quantity: 3

Code Information:

Model Number: S-05-100-120-G3; Lot Number 01049037

Distribution Pattern:

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

Voluntary or Mandated:

Voluntary: Firm initiated