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Bd alaris™ syringe pumps

Official notice

20 Feb 2026

Last checked

20 Feb 2026

Critical riskHealth Canada
Watch Bd Switzerland Sarl

An official Health Canada notice concerns Bd alaris™ syringe pumps. BD has identified through an internal investigation that the BD Alaris™ syringe pumps may develop a mechanical anomaly on the linear potentiometer if the device is not stored in the correct position. The syringe plunger moves along the linear potentiometer component during infusion. This is an internal component and not readily visible to the clinical user. If this anomaly occurs, it can lead to incorrect sensor readings, which may trigger error codes PL3, PL8, or PL9. These PL error codes are an intentional design feature that notify the clinical user that the syringe pump has detected an internal malfunction and can occur for a number of reasons. The PL3/PL8/PL9 error codes result in the syringe pump issuing an error message along with a red illuminated beacon, and a high priority alarm tone. If an infusion is in progress, it will stop. The error code will be displayed on the syringe pump as , see below image example of a PL9 error code. Published 2026-02-20.

What to do now

Contact the manufacturer if you require additional information.

Recall number

81631

Official notice

2026-02-20

The hazard

BD has identified through an internal investigation that the BD Alaris™ syringe pumps may develop a mechanical anomaly on the linear potentiometer if the device is not stored in the correct position. The syringe plunger moves along the linear potentiometer component during infusion. This is an internal component and not readily visible to the clinical user. If this anomaly occurs, it can lead to incorrect sensor readings, which may trigger error codes PL3, PL8, or PL9. These PL error codes are an intentional design feature that notify the clinical user that the syringe pump has detected an internal malfunction and can occur for a number of reasons. The PL3/PL8/PL9 error codes result in the syringe pump issuing an error message along with a red illuminated beacon, and a high priority alarm tone. If an infusion is in progress, it will stop. The error code will be displayed on the syringe pump as , see below image example of a PL9 error code.

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.

Skus

8002MED01-G, 8002TIG01-G, 8002TIG03-G, 8005PK201, 8005TIG01, 8005TIG03, 8003TIG01-G, 8003TIG03-G, 8003MED01-G

Other

RA RA-81631

Model Numbers

8002MED01-G, 8002TIG01-G, 8002TIG03-G, 8005PK201, 8005TIG01, 8005TIG03, 8003TIG01-G, 8003TIG03-G, 8003MED01-G

Recall Numbers

81631

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Affected products

Product 1

Lot or serial number - More than 10 numbers, contact manufacturer., Model or catalogue number - 8002MED01-G

Product 2

Lot or serial number - More than 10 numbers, contact manufacturer., Model or catalogue number - 8002TIG01-G

Product 3

Lot or serial number - More than 10 numbers, contact manufacturer., Model or catalogue number - 8002TIG03-G

Product 4

Lot or serial number - More than 10 numbers, contact manufacturer., Model or catalogue number - 8005PK201

Product 5

Lot or serial number - More than 10 numbers, contact manufacturer., Model or catalogue number - 8005TIG01

Product 6

Lot or serial number - More than 10 numbers, contact manufacturer., Model or catalogue number - 8005TIG03

Product 7

Lot or serial number - More than 10 numbers, contact manufacturer., Model or catalogue number - 8003TIG01-G

Product 8

Lot or serial number - More than 10 numbers, contact manufacturer., Model or catalogue number - 8003TIG03-G

Product 9

Lot or serial number - More than 10 numbers, contact manufacturer., Model or catalogue number - 8003MED01-G

Risk / hazard

BD has identified through an internal investigation that the BD Alaris™ syringe pumps may develop a mechanical anomaly on the linear potentiometer if the device is not stored in the correct position. The syringe plunger moves along the linear potentiometer component during infusion. This is an internal component and not readily visible to the clinical user. If this anomaly occurs, it can lead to incorrect sensor readings, which may trigger error codes PL3, PL8, or PL9. These PL error codes are an intentional design feature that notify the clinical user that the syringe pump has detected an internal malfunction and can occur for a number of reasons. The PL3/PL8/PL9 error codes result in the syringe pump issuing an error message along with a red illuminated beacon, and a high priority alarm tone. If an infusion is in progress, it will stop. The error code will be displayed on the syringe pump as , see below image example of a PL9 error code.

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

Bd Switzerland Sarl

Manufacturer

Not provided

Phone

Not provided

Brand: Bd Switzerland Sarl.

Source & status

Source

Health Canada

Tier

official

Category

HEALTH

Classification

Type II

App estimate

critical

Recall details

Recall number

81631

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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