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Recall Observatory FDA recall evidence

Device product

Mevatron M2/Primus Mid-Energy PRIMUS HI

Z-1489-2017

February 14, 2017

Class II

Product summary

Firm
Siemens Medical Solutions USA, Inc
Event
Event 76712
Status
Terminated
Classification
Class II
Quantity
80 systems
Official record key
device-enforcement:Z-1489-2017

Official wording

Reason: Software update

Code information: Device Model# 1940035, 4504200

Distribution pattern: Distributed throughout the United States

Derived failure modes

  • Unknown

    reason.no_named_rule · v1.0.0

    Software update