Health product recall

Bd Alaris

Last updated

Summary

Product
Bd Alaris
Issue
Medical devices - Unauthorised device
What to do

Contact the manufacturer if you require additional information.

Affected products

Affected Products

Lot or Serial Number

Model or catalog number

Alaris Auto-Id Module

Not applicable.

8100

Bd Alaris Pump Module

Not applicable.

8300

Bd Alaris Etco2 Module

Not applicable.

8600

Bd Alaris Pcu

Not applicable.

8000, 8015 (V10.5)

Alaris Pca Module

Not applicable.

8120

Bd Alaris Syringe Module

Not applicable.

8110 (V10.5)

Issue

Recall is being initiated to notify customers to the risk of the use and installation of unauthorized, third-party parts on the Alaris system.

Recall start date: Feb 7, 2022

Additional information

Details
Original published date: 2022-02-28
Alert / recall type
Health product recall
Category
Health product - Medical device - 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
General public
Health professionals
Hospitals
Recall class
Type II
Identification number
RA-63948