CareFusion Recalls

2 recalls found for CareFusion. Check if any of your products are affected.

Health & Personal Care
HIGH
FDA DRUG

CareFusion Recalls ChloraPrep Swabsticks Due to Sterility Concerns

CareFusion 213, LLC recalled 106,400 units of ChloraPrep Triple Swabsticks on December 17, 2025. The recall occurred due to a lack of assurance of sterility. Consumers must stop using the product immediately and contact CareFusion for guidance.

ChloraPrep
Lack of
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Health & Personal Care
HIGH
FDA DEVICE

CareFusion 303 BD Alaris Infusion Sets Recalled for Flow, Bolus Accuracy Issues (2025)

CareFusion 303 BD Alaris infusion pump modules and compatible infusion sets are recalled nationwide in the U.S. and multiple international markets. The recall covers reference numbers including C24101E and 10015414 and related SmartSite components. The defect may cause flow rate and bolus accuracy deviations, and incorrect occlusion timing. Stop using the device and follow recall instructions from

CareFusion
Infusion pump
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Brand Statistics

Total Recalls
2
Pages
1

Related Brands

ChloraPrepBDBD AlarisCareFusion 303