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Recall Observatory FDA recall evidence

Device product

LVP software of the Ivenix Infusion System (IIS), LVP-SW-0004

Z-1282-2024

September 16, 2022

Class II

Product summary

Firm
Fresenius Kabi USA, LLC
Event
Event 93958
Status
Completed
Classification
Class II
Quantity
3
Official record key
device-enforcement:Z-1282-2024

Official wording

Reason: Retroactively reported correction from 2022: A software defect may cause an incorrect (Fail-Stop) Alarm when an administration set is loaded with an upstream occlusion present, resulting in a non-recoverable (Fail-Stop) Pump Problem alarm. This may lead to delay of therapy, and patient may experience from no to minimal to serious harm. This issue was resolved in all fielded product in software version 5.2.1, which was installed in September 2022.

Code information: UDI-DI 00811505030122 Software versions 5.0.1 and earlier.

Distribution pattern: US Nationwide distribution in the states of WI and NJ.

Derived failure modes

  • Device software or design

    reason.device_software_design · v1.0.0

    software defect may cause an incorrect