Device recall

Z-1479-2018: Medtronic DxTerity Diagnostic Catheter, JL 4.0, REF DXT5JL40, marked with 6F…

FDA device recall · Class II · Medtronic Vascular

Key facts

Recall number (Z-number) Z-1479-2018
Recall event 79591
Product Medtronic DxTerity Diagnostic Catheter, JL 4.0, REF DXT5JL40, marked with 6F color code on box.
Product code DQO
Recalling firm Medtronic Vascular
Recall class Class II
Status Terminated
Termination date May 7, 2021
510(k) numbers K161287
FEI number 1220452

At a glance

  • 1–9 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)