FDASeptember 15, 2023device

BD Alaris PCU REF 8015

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

The hazard

Alaris PCA Module 8120, Patient Controlled Analgesia infusion pump: compatible syringes labeling contains syringes that have not been validated.

What to do

FDA enforcement status: Ongoing

Brands named

carefusion 303carefusion

UPCs

108854035160301088540351531610885403812033108854035152861088540381202610885403515293108854034942911088540351530910885403812002

Recall history

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

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