
No image published for this recall
Alaris™ syringe pump mk4
Official notice
30 Oct 2023
Last checked
30 Oct 2023
An official Health Canada notice concerns Alaris™ syringe pump mk4. BD is issuing a notification to inform customers that Cardinal Health branded Monoject™ syringes have not been validated for use with the BD Alaris™ infusion devices. BD has validated Covidien branded Monoject™ syringes for use with the BD Alaris™ infusion devices. Cardinal Health, rebranded its syringes from Covidien Monoject™ to Cardinal Health Monoject™ and retained the original Covidien SKU numbers. BD's investigation determined that there may differences in syringe dimensions associated with these changes that may impact BD Alaris infusion devices. Recall start date: October 12, 2023 Published 2023-10-30.
What to do now
Contact the manufacturer if you require additional information.
Recall number
74492
Official notice
2023-10-30
The hazard
The hazard
BD is issuing a notification to inform customers that Cardinal Health branded Monoject™ syringes have not been validated for use with the BD Alaris™ infusion devices. BD has validated Covidien branded Monoject™ syringes for use with the BD Alaris™ infusion devices. Cardinal Health, rebranded its syringes from Covidien Monoject™ to Cardinal Health Monoject™ and retained the original Covidien SKU numbers. BD's investigation determined that there may differences in syringe dimensions associated with these changes that may impact BD Alaris infusion devices. Recall start date: October 12, 2023
How to check if you're affected
How to check if you're affected
Compare the VIN on your vehicle against the official list. If your VIN is listed, follow the official notice.
Recall Numbers
Checked manually this time?
The app watches your VIN and alerts you automatically next time — no searching, no checking back.
Turn on automatic VIN checksAffected products
Affected products
Product 1
Product 2
Risk / hazard
Where it was sold
Where it was sold
The source does not list specific retailers. See the official notice for where affected vehicles were sold.
Location 1
Affected area 1
Company & contacts
Company & contacts
Brand
Manufacturer
Phone
Brand: Bd Switzerland Sarl, Alaris™ Syringe Pump Mk4.
Source & status
Source & status
Source
Tier
Category
Classification
App estimate
Recall details
Recall details
Recall number
Classification
Source tier
Documents, notices & source
See the official notice and source documents for full details.
View full official noticeRelated recalls

Bd maxplus ™ connector minibore extension set

Bd alaris™ syringe pumps

Bd alaris™ pump module and subset of compatible pump infusion sets

Bd texium™ components

Alaris™ pump infusion set low sorbing tubing (pe lined) back check valve 2 smartsite™ y-site(s)

Alaris™ gh plus guardrails™ syringe pump

Bd smartsite low sorbing extension set

Bd infusion sets

Bd maxguardtm extension sets

Glidesheath slender® introducer sheath

Importation of chinese-authorized ifosfamide for injection due to the current shortage of canadian-authorized ifex (ifosfamide for injection)

Corneat kpro
Weekly recall digest
Get next week's recalls before you need them.
One email every Monday — official-source recalls for your country, and nothing else. Unsubscribe from any email.
The digest is the slow lane — one email a week. For instant, severity-gated alerts the moment a notice is published, get the app.
This recall was published 30 Oct 2023. The next one won't wait for you to search.
RecallScope watches official sources for the brands and VINs you follow, and alerts you the moment a new notice is published.