Device recall

Z-1023-2013: 20-Pole Eco Cable, Catalog #EM-5050-060 Product Usage: The 20-Pole Eco Cable is…

FDA device recall · Class II · Biosense Webster, Inc.

Key facts

Recall number (Z-number) Z-1023-2013
Recall event 64579
Product 20-Pole Eco Cable, Catalog #EM-5050-060 Product Usage: The 20-Pole Eco Cable is intended to be used as an interface cable between the LASSO NAV Eco Catheter and CARTO 3 System.
Product code DQK
Recalling firm Biosense Webster, Inc.
Recall class Class II
Status Terminated
Termination date Oct 17, 2013
510(k) numbers K120550
FEI number 3003113629

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)