Official recall record

Alaris™ Pump Module & BD Alaris™ Pump Module

Health Canada — Medical Devices · 2025-07-22 · CanadaType I

Issuing authority: Health Canada — Medical Devices
Published: 2025-07-22
Country of alert: Canada
Alert level: Type I
Alert type: recall

What the authority reported

BD has become aware via customer complaints of customer/third-party continued usage of previously recalled bezel kit assemblies to service Alaris™ and BD Alaris™pump modules. These affected bezel kit assemblies were manufactured with fr-110 resin between April 2011 and June 2017 and should not be used in servicing as these may present with separated and/or broken bezel bosses that can lead to free flow, over infusion, under infusion or interruption of infusion. Recall start date: July 16, 2025

What to do

Follow the instructions in the official notice — recall remedies (refund, repair, replacement, or disposal) are defined by the issuing authority and the responsible business, and they differ per recall. Do not rely on summaries, including this one.

Verify at the source: Health Canada — Medical Devices — official record →
Record last checked against the registry on 2026-05-31.

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