Official recall record
BD Alaris™ Pump Module
- Issuing authority
- Health Canada — Medical Devices
- Published
- 2025-10-29
- Country of alert
- Canada
- Alert level
- Type II
- Alert type
- recall
What the authority reported
BD was made aware via customer complaints that dropping the BD Alaris™ Pump Module may cause damage to internal components that may not be apparent or readily visible. More specifically, drops or severe jarring may damage the BD Alaris™ Pump Module bezel assembly, which provides the mechanical foundation for critical pumping components. This damage can cause under-infusion, over-infusion, unregulated flow or failure of the BD Alaris™ Pump Module to calibrate.
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.
Record last checked against the registry on 2026-05-31.
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