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
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