Device recall

Z-2739-2016: Centricity Enterprise Archive is a software product for receiving, archiving and…

FDA device recall · Class II · Ge Healthcare It

Key facts

Recall number (Z-number) Z-2739-2016
Recall event 64761
Product Centricity Enterprise Archive is a software product for receiving, archiving and sending of medical data. Qualified system administrators install, monitor and maintain the system. DICOM devices (e.g. modalities, workstations) communicate with the archive using the DICOM protocol (published by…
Product code LMB
Recalling firm Ge Healthcare It
Recall class Class II
Status Terminated
Termination date Jan 11, 2017
FEI number 3004526608

At a glance

  • None Linked 510(k)s
  • 1–9 Products in the same recall event
  • 10–99 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)