Device recall

Z-1706-2014: Kenex Radiation Shield and surgical lamps installed with GE Healthcare…

FDA device recall · Class II · GE Healthcare, LLC

Key facts

Recall number (Z-number) Z-1706-2014
Recall event 68219
Product Kenex Radiation Shield and surgical lamps installed with GE Healthcare Interventional, Surgery, CT and X-Ray Imaging systems. Kenex Suspension installed with Radiation shield and lamp with following model numbers…
Product code KPY
Recalling firm GE Healthcare, LLC
Recall class Class II
Status Terminated
Termination date Feb 25, 2015
FEI number 2126677

At a glance

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