Device recall

Z-0213-2009: GE Healthcare, Mobile Care Server used in conjunction with Web Viewer, Pocket…

FDA device recall · Class II · GE Healthcare

Key facts

Recall number (Z-number) Z-0213-2009
Recall event 49440
Product GE Healthcare, Mobile Care Server used in conjunction with Web Viewer, Pocket Viewer, and Cellular Viewer WIT with L-WEB05 software. GE Healthcare 8200 West Tower Avenue, Milwaukee, WI 53223 Mobile Care Server maintains and coordinates the network connections between the devices in the Datex-Ohmeda…
Product code MSX
Recalling firm GE Healthcare
Recall class Class II
Status Terminated
Termination date Nov 24, 2015
510(k) numbers K061994
FEI number 3004526608

At a glance

  • 1–9 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)