Device recall

Z-1029-2011: SEQUENCER for Mosaiq interfaced to Electa SL75-5 machines. Sequencer Verify and…

FDA device recall · Class II · Impac Medical Systems Inc

Key facts

Recall number (Z-number) Z-1029-2011
Recall event 55087
Product SEQUENCER for Mosaiq interfaced to Electa SL75-5 machines. Sequencer Verify and Record System is to assist in the process of patient treatment on a radiotherapy treatment machine with software control.
Product code IYE
Recalling firm Impac Medical Systems Inc
Recall class Class II
Status Terminated
Termination date Apr 6, 2011
510(k) numbers K981313
FEI number 1000123805

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

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