Bd Alaris
Brand(s)
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:
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
General public
Health professionals
Hospitals
Recall class
Type II
Identification number
RA-63948
Get notified
Receive notifications for new and updated recalls and alerts by category.