ProductGuru Recalls

Official recall record

Alaris™ Syringe Pump MK4

Health Canada — Medical Devices · 2023-10-30 · CanadaType I
Issuing authority
Health Canada — Medical Devices
Published
2023-10-30
Country of alert
Canada
Alert level
Type I
Alert type
recall

What the authority reported

BD is issuing a notification to inform customers that Cardinal Health branded Monoject™ syringes have not been validated for use with the BD Alaris™ infusion devices. BD has validated Covidien branded Monoject™ syringes for use with the BD Alaris™ infusion devices. Cardinal Health, rebranded its syringes from Covidien Monoject™ to Cardinal Health Monoject™ and retained the original Covidien SKU numbers. BD's investigation determined that there may differences in syringe dimensions associated with these changes that may impact BD Alaris infusion devices. Recall start date: October 12, 2023

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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