FDAApril 18, 2024device

Alaris Pump Infusion Set Low Sorbing Tubing (PE Lined) Back Check Valve 2 SmartSite Y Sites REF 10013072 Tubing set used for delivery of fluids, medication, blood and blood products.

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

The hazard

Due to infusion set tubing drip chamber becoming detached from the tubing potentially causing delays in treatment, or unintentionally exposing users to harsh infusates.

What to do

FDA enforcement status: Ongoing

Brands named

bd switzerland sarl

UPCs

07613203021210

Recall history

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

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