Device recall

Z-0370-2012: Varian brand Eclipse Release 10 with RT Chart Release 10 (Client Build 10.0.28…

FDA device recall · Class II · Varian Medical Systems, Inc. Oncology Systems

Key facts

Recall number (Z-number) Z-0370-2012
Recall event 60441
Product Varian brand Eclipse Release 10 with RT Chart Release 10 (Client Build 10.0.28 or Build 10.0.34), An Eclipse Treatment Planning System used with ARIA Radiation Oncology (RT Chart module), Reference/FSCA Identifier: CP-05277, Model Number: H48; Product is manufactured and distributed by Varian…
Product code MUJ
Recalling firm Varian Medical Systems, Inc. Oncology Systems
Recall class Class II
Status Terminated
Termination date Jun 6, 2014
510(k) numbers K091492
FEI number 2916710

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)