Product Wiki · Recalls · Health Canada — Medical Devices

Alaris™ Syringe Pump MK4 — recall 74492

Health Canada — Medical Devices · Canada · 2023-10-30 · Type I

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Agency
Health Canada — Medical Devices
Recall identifier
74492
Date of alert
2023-10-30
Country / jurisdiction
Canada
Risk level
Type I
Risk type
recall
Product category
General hospital and personal use
Product type
Medical devices
Reported risk: 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
Primary source: https://recalls-rappels.canada.ca/en/alert-recall/alaristm-syringe-pump-mk4

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ProductGuru indexes recall and safety-alert records from ~30 public agency registries. We are not lawyers, regulators or product-safety consultants. This page restates what the named agency published; consult the primary source above (or qualified counsel in your jurisdiction) before any commercial, medical or safety decision.