FDASeptember 15, 2023device

BD Alaris Syringe Module, REF 8110

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

10885403516047108854035153231088540381104310885403515262108854038110121088540351527910885403424267

Recall history

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

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BD Alaris Syringe Module, REF 8110 — Recall Details · AllClear