FDA MedWatch Safety AlertsOriginal article
Infusion Set Recall: BD and CareFusion 303, Inc. Remove BD Alaris Pump Infusion Sets
RegulatoryBD Alaris Pump Infusion SetsBD Alaris Pump Module model 8100Negative
AI Analysis
Summary
BD and its subsidiary CareFusion 303 are removing and discontinuing BD Alaris Pump Infusion Sets, per an FDA MedWatch notice. The Alaris Pump Module model 8100 also has updated performance data.
Outcome Details
BD and CareFusion 303 are removing and discontinuing BD Alaris Pump Infusion Sets; Alaris Pump Module model 8100 has updated performance data.
Importance:5/10
Sentiment:
-0.40
recallmedical deviceinfusion pumpFDA MedWatchproduct discontinuationAlaris
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Published by FDA MedWatch Safety Alerts on October 14, 2026 4:00 AM