Device recall

Z-0213-2008: Ximatron Digital Imaging (Ximavision), V 7.5.51 with Service Pack (SP), Oncology…

FDA device recall · Class II · Varian Medical Systems Inc

Key facts

Recall number (Z-number) Z-0213-2008
Recall event 38376
Product Ximatron Digital Imaging (Ximavision), V 7.5.51 with Service Pack (SP), Oncology Information System, Varian Medical Systems
Product code KPQ
Recalling firm Varian Medical Systems Inc
Recall class Class II
Status Terminated
Termination date Feb 4, 2008
510(k) numbers K851653
FEI number 2916710

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)