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Recall Observatory FDA recall evidence

Device product

HAMILTON-C6, REF: 160021

Z-1429-2023

March 14, 2023

Class II

Product summary

Firm
Hamilton Medical AG
Event
Event 91925
Status
Ongoing
Classification
Class II
Quantity
103
Official record key
device-enforcement:Z-1429-2023

Official wording

Reason: Software error causes, safety ventilation, in which ventilation continues in the "safety ventilation" mode with audible/visible alarm - patient inputs are not monitored, if the following coincide 1) A mode change to an adaptive mode (ASV, APVcmv, APVsimv, INTELLiVENT-ASV, (S)CMV+, SIMV+), and 2) The controller and/or humidifier is connected to the ventilator and is operational.

Code information: Software Version: 1.2.1, UDI-DI: 07630002808590

Distribution pattern: US Nationwide distribution in the states of CA, MA, ID, NC, GA, FL, NV, PA, MO, KS, SC, NY, NM, WY, VA.

Derived failure modes

  • Device software or design

    reason.device_software_design · v1.0.0

    Software error