Recall Monitor
Health ProductsType I recall

Alaris™ Pump Module & BD Alaris™ Pump Module

· Published by Health Canada · Official notice

Details

Alert type: Health product recall
Category: Health products - Medical devices - General hospital and personal use
Product: Alaris™ Pump Module & BD Alaris™ Pump Module
Issue: Medical devices - Device compatibility
What to do: Contact the manufacturer if you require additional information.
Audience: Healthcare
Recall class: Type I
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Products

Affected productsLot or serial numberModel or catalogue number
Alaris™ Pump Module & BD Alaris™ Pump ModuleMore than 10 numbers, contact manufacturer.8100

Issue

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

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