Health product recall

BD Alaris PCU

Last updated

Summary

Product
BD Alaris PCU
Issue
Medical devices - Performance
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

BD Alaris PCU

More than 10 numbers, contact manufacturer.

8015

Issue

BD  has identified an increase in bent contacts on new female/left IUI connectors on devices and spare parts manufactured between Jan 01, 2023 and June 06, 2024. BD was made aware of this issue through complaints identified during the device check-in process and has not received any reports of this issue occurring during patient use. A defective pin on certain female/left IUI connectors that are not detected prior to use could result in an inoperable device or an operable device where adjoining device cannot be powered on at start up.

Recall start date: August 16, 2024 

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 II
Identification number
RA-76031

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