FDAMay 2, 2025device

LifeShield Drug Library Management (DLM), LifeShield Infusion Safety Software SUite v2.1 and v2.2

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

Firm has identified Drug Library Management defects in the software: 1) DLM software does not allow user to create percentage dose rate or rate change values with certain limits, potentially resulting in over-delivery to patient. 2) An unauthorized user may modify and approve a drug library, potentially leading to incorrect program parameters being used for therapy.

What to do

FDA enforcement status: Ongoing

Brands named

icu medicalicu

UPCs

00887709122802

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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