Device recall

Z-0083-2014: Valiant Thoracic Stent Graft with Captivia Delivery System, Talent Thoracic…

FDA device recall · Class II · Medtronic Vascular, Inc.

Key facts

Recall number (Z-number) Z-0083-2014
Recall event 66322
Product Valiant Thoracic Stent Graft with Captivia Delivery System, Talent Thoracic Stent Graft with the Captivia Delivery System.
Product code MIH
Recalling firm Medtronic Vascular, Inc.
Recall class Class II
Status Terminated
Termination date Oct 25, 2013
PMA numbers P100040, P100040/P070
FEI number 3005364322

At a glance

  • None Linked 510(k)s
  • 1–9 Products in the same recall event
  • 100–999 Recalled products with this product code

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

About FDA device recalls (products)

Each recalled device product receives a Z-number. Recall details such as root cause, distribution and firm actions are available in Orca1.

Source: U.S. Food and Drug Administration (FDA), Medical Device Recalls database

Browse all FDA device recalls (products)