Device recall

Z-1403-2010: GE Centricity Web Diagnostic (WebDX) software; GE Healthcare Integrated IT…

FDA device recall · Class II · Ge Healthcare It

Key facts

Recall number (Z-number) Z-1403-2010
Recall event 55037
Product GE Centricity Web Diagnostic (WebDX) software; GE Healthcare Integrated IT Solutions, Barrington, IL 60010. Device that receives, stores and communicates medical images and data from various imaging sources.
Product code LLZ
Recalling firm Ge Healthcare It
Recall class Class II
Status Terminated
Termination date Nov 15, 2010
510(k) numbers K083018
FEI number 3004526608

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)