BD Alaris™ Infusion Devices
Brand(s)
Summary
Contact the manufacturer if you require additional information.
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
Carefusion 303, Inc.
10020 Pacific Mesa Blvd., San Diego, California, United States, 92121-2733
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