Alaris™ Pump Module & BD Alaris™ Pump Module
Brand(s)
Last updated
Summary
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
Affected products
| Affected products | Lot or serial number | Model or catalogue number |
|---|---|---|
| Alaris™ Pump Module & BD Alaris™ Pump Module | More 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
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 |
Published by
Health Canada
Audience
Healthcare
Recall class
Type I
Identification number
RA-77754
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