FDANovember 24, 2025device

LifeShield Drug Library Management (DLM); LifeShield Infusion Safety Software Suite v2.2 List Number 17003-02

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

The hazard

For certain customers, the Change Summary review option ceases to operate as expected for any migrated library after the migration has been completed. Users must use alternate methods to review changes. Failure to do so may lead in over delivery, under delivery, or delay in setup on the infusion pump.

What to do

FDA enforcement status: Ongoing

Brands named

icu medicalicu

UPCs

00887709127227

Recall history

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

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