FDASeptember 11, 2025device

BD Alaris Pump Infusion Sets for the following reference numbers: C24101E, Amber Tubing, 15 Micron Filter, 0.2 Micron Filter, SmartSite Y-Site 10015414, 180 Micron Filter 2447-0007, Ball Valve SmartSite Port (Burette) 2 SmartSites Y-Sites 24201-0007, 2 SmartSite Y-sites 10012645, Back Check Valve...

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

The hazard

Infusion pump module used with compatible pump infusion sets may perform outside the established performance ranges for flow rate and bolus accuracy, downstream and upstream occlusion time to alarm, and post-occlusion bolos volume.

What to do

FDA enforcement status: Ongoing

Brands named

carefusion 303carefusion

UPCs

108854032355281088540323399910885403235078108854034763411088540323375376132030209921088540323230576132030124921088540346396910885403276026761320302115910885403232312

Recall history

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

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BD Alaris Pump Infusion Sets for the following reference numbers: C24101E, Amber Tubing, 15 Micron Filter, 0.2 Micron Filter, SmartSite Y-Site 10015414, 180 Micron Filter 2447-0007, Ball Valve SmartSite Port (Burette) 2 SmartSites Y-Sites 24201-0007, 2 SmartSite Y-sites 10012645, Back Check Valve... — Recall Details · AllClear