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Recall Observatory FDA recall evidence

Device product

Draeger Infinity M300 and M300+, for use with the ICS to monitor ECG and pulse oximetry on ambulatory and non-ambulatory adult and pediatric patients using wireless communication over the Infinity patient monitoring network,

Z-1472-2023

April 05, 2023

Class II

Product summary

Firm
Draeger Medical Systems, Inc.
Event
Event 91938
Status
Ongoing
Classification
Class II
Quantity
19,429 systems
Official record key
device-enforcement:Z-1472-2023

Official wording

Reason: The software on the Infinity CentralStation drops peaks on narrow waveforms causing the Infinity M300 to fail to meet Frequency and Impulse Response requirements. In this condition, ECG waveforms with unusually narrow and/or high frequency QRS may be displayed or printed with QRS amplitudes intermittently lower than actual.

Code information: UDI-DI: 04049098048989 (M300), 04049098095778 (M300+); All Systems Running Software versions: VG2.4 and lower

Distribution pattern: Worldwide - US Nationwide distribution.

Derived failure modes

  • Device software or design

    reason.device_software_design · v1.0.0

    software on the Infinity CentralStation drops peaks on narrow waveforms causing the Infinity M300 to fail to