Device recall

Z-0507-2015: TomoTherapy Treatment System with software versions 2.0.1 / 2.0.2 / 2.0.3/…

FDA device recall · Class II · TomoTherapy Incorporated

Key facts

Recall number (Z-number) Z-0507-2015
Recall event 69854
Product TomoTherapy Treatment System with software versions 2.0.1 / 2.0.2 / 2.0.3/ (Hi:Art 5.0.1 / 5.0.2 / 5.0.3)
Product code IYE
Recalling firm TomoTherapy Incorporated
Recall class Class II
Status Terminated
Termination date Jul 17, 2015
510(k) numbers K121934
FEI number 3003873069

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)