FDASeptember 15, 2023device

Alaris PCA Module 8120

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

10885403516023108854035152311088540380154910885403515248108854038015321088540351522410885403801518

Recall history

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

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