Medical device recalls

BD recalls Alaris — Alaris Pump Module Model 8100 and Certain Alaris Pump Infusion Sets

Recall date
July 18, 2019
Source
U.S. Food & Drug Administration (FDA) — recall announcement
Brand / firm
BD, Alaris

Why it was recalled

Weakening of the plastic can lead to damage or separation of the bezel posts which can cause issues with infusion, or unintended delivery of medication when pump module is not in running status — Defect

What was recalled

Alaris Pump Module Model 8100 and Certain Alaris Pump Infusion Sets

Read the official recall notice →

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More recalls from: BD, Alaris