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Bd alaris pcu

Official notice

11 Sept 2024

Last checked

11 Sept 2024

Medium riskHealth Canada
Watch Carefusion 303

An official Health Canada notice concerns Bd alaris pcu. BD has identified an increase in bent contacts on new female/left IUI connectors on devices and spare parts manufactured between Jan 01, 2023 and June 06, 2024. BD was made aware of this issue through complaints identified during the device check-in process and has not received any reports of this issue occurring during patient use. A defective pin on certain female/left IUI connectors that are not detected prior to use could result in an inoperable device or an operable device where adjoining device cannot be powered on at start up. Recall start date: August 16, 2024 Published 2024-09-11.

What to do now

Contact the manufacturer if you require additional information.

Recall number

76031

Official notice

2024-09-11

The hazard

BD has identified an increase in bent contacts on new female/left IUI connectors on devices and spare parts manufactured between Jan 01, 2023 and June 06, 2024. BD was made aware of this issue through complaints identified during the device check-in process and has not received any reports of this issue occurring during patient use. A defective pin on certain female/left IUI connectors that are not detected prior to use could result in an inoperable device or an operable device where adjoining device cannot be powered on at start up. Recall start date: August 16, 2024

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

76031

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Affected products

Product 1

Affected products - BD Alaris PCU, Lot or serial number - More than 10 numbers, contact manufacturer., Model or catalogue number - 8015

Risk / hazard

BD has identified an increase in bent contacts on new female/left IUI connectors on devices and spare parts manufactured between Jan 01, 2023 and June 06, 2024. BD was made aware of this issue through complaints identified during the device check-in process and has not received any reports of this issue occurring during patient use. A defective pin on certain female/left IUI connectors that are not detected prior to use could result in an inoperable device or an operable device where adjoining device cannot be powered on at start up. Recall start date: August 16, 2024

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 Pcu

Manufacturer

Not provided

Phone

Not provided

Brand: Carefusion 303, Bd Alaris Pcu.

Source & status

Source

Health Canada

Tier

official

Category

HEALTH

Classification

Type II

App estimate

medium

Recall details

Recall number

76031

Classification

Type II

Source tier

official

Documents, notices & source

See the official notice and source documents for full details.

View full official notice
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