Health product recall

BD Alaris™ Infusion Devices

Last updated

Summary

Product
BD Alaris™ Infusion Devices
Issue
Medical devices - Device compatibility
What to do

Contact the manufacturer if you require additional information. 

Audience
Healthcare

Affected products

Affected products Lot or serial number Model or catalog number
BD Alaris™ PC Unit More than 10 numbers, contact manufacturer. 8015
BD Alaris™ Syringe Module More than 10 numbers, contact manufacturer. 8110
Alaris™ Patient-Controlled Analgesia (PCA) Module More than 10 numbers, contact manufacturer. 8120

Issue

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

Additional information

Details
Original published date:
Alert / recall type
Health product recall
Category
Health products - Medical devices - General hospital and personal use
Companies

Carefusion 303, Inc.

10020 Pacific Mesa Blvd., San Diego, California, United States, 92121-2733

Published by
Health Canada
Audience
Healthcare
Recall class
Type I
Identification number
RA-74491