BD Alaris™ Pump Module
Brand(s)
Last updated
Summary
Product
BD Alaris™ Pump Module
Issue
Medical devices - Performance
What to do
Contact the manufacturer if you require additional information.
Audience
Healthcare
Industry
Affected products
| Affected products | Lot or serial number | Model or catalogue number |
|---|---|---|
| BD Alaris™ Pump Module | More than 10 numbers, contact manufacturer. | 8100 |
Issue
BD was made aware via customer complaints that dropping the BD Alaris™ Pump Module may cause damage to internal components that may not be apparent or readily visible. More specifically, drops or severe jarring may damage the BD Alaris™ Pump Module bezel assembly, which provides the mechanical foundation for critical pumping components. This damage can cause under-infusion, over-infusion, unregulated flow or failure of the BD Alaris™ Pump Module to calibrate.
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
Industry
Recall class
Type II
Recall date
Identification number
RA-78411
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