FDA MedWatch Safety AlertsOriginal article
Infusion Set Recall: BD and CareFusion 303, Inc. Remove BD Alaris Pump Infusion Sets
RegulatoryBD Alaris Pump Infusion SetsAlaris Pump Module model 8100Negative
AI Analysis
Summary
BD and CareFusion 303 are removing and discontinuing BD Alaris Pump Infusion Sets, with updated performance data provided for the Alaris Pump Module model 8100. This regulatory action affects the infusion pump product line.
Outcome Details
Product recall and discontinuation
Importance:6/10
Sentiment:
-0.80
product recallmedical deviceinfusion pumpFDA MedWatchproduct discontinuation
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Published by FDA MedWatch Safety Alerts on October 5, 2026 4:00 AM