Recalled BD Alaris pump infusion sets may be packed inside some Cardinal Health procedure kits, the Food and Drug Administration warned on Oct. 20. The agency issued an early alert on the Presource kits, saying they may contain sets covered by BD's Class I recall, FDA's most serious category.
The affected sets can cause unpredictable pump behavior, including over-infusion, under-infusion, or failure to infuse, according to the FDA. As of Aug. 19, 2026, BD had not reported any serious injuries or deaths linked to the issue.
