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Bd alaris™ infusion devices

Official notice

30 Oct 2023

Last checked

30 Oct 2023

High riskHealth Canada
Watch Carefusion 303

An official Health Canada notice concerns Bd alaris™ infusion devices. 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

74491

Official notice

2023-10-30

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

Compare the VIN on your vehicle against the official list. If your VIN is listed, follow the official notice.

Recall Numbers

74491

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Affected products

Product 1

Affected products - BD Alaris™ PC Unit, Lot or serial number - More than 10 numbers, contact manufacturer., Model or catalog number - 8015

Product 2

Affected products - BD Alaris™ Syringe Module, Lot or serial number - More than 10 numbers, contact manufacturer., Model or catalog number - 8110

Product 3

Affected products - Alaris™ Patient-Controlled Analgesia (PCA) Module, Lot or serial number - More than 10 numbers, contact manufacturer., Model or catalog number - 8120

Risk / 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

Where it was sold

The source does not list specific retailers. See the official notice for where affected vehicles were sold.

Location 1

CA · Canada

Affected area 1

CA · Canada

Company & contacts

Brand

Carefusion 303, Bd Alaris™ Infusion Devices

Manufacturer

Not provided

Phone

Not provided

Brand: Carefusion 303, Bd Alaris™ Infusion Devices.

Source & status

Source

Health Canada

Tier

official

Category

HEALTH

Classification

Type I

App estimate

high

Recall details

Recall number

74491

Classification

Type I

Source tier

official

Documents, notices & source

See the official notice and source documents for full details.

View full official notice
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