FDADecember 19, 2025device

Pulsator Arterial Blood Sampling Kit, Item Numbers 4044EG-1 4080P-2 4084P-1 4080PE 4080PG

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

The hazard

Affected lots of syringes may have a crack on the syringe collar, which may lead to delayed or repeated blood draw/fluid delivery. This issue may also lead to blood leakage during sampling of arterial blood or leakage during fluid delivery.

What to do

FDA enforcement status: Ongoing

Brands named

icu medicalicu

UPCs

303516880730626141992615622830351688006176303516880295403035168803915030351688081173

Recall history

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

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