Device recall

Z-1910-2019: Centricity Universal Viewer 6.0 Is a device that displays medical images and…

FDA device recall · Class II · GE Healthcare, LLC

Key facts

Recall number (Z-number) Z-1910-2019
Recall event 82998
Product Centricity Universal Viewer 6.0 Is a device that displays medical images and data from various imaging sources, and from other healthcare information sources.
Product code LLZ
Recalling firm GE Healthcare, LLC
Recall class Class II
Status Terminated
Termination date Apr 14, 2023
510(k) numbers K150420, K182419
FEI number 2126677

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)