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Medrad® centargo injection system

Official notice

28 Jan 2025

Last checked

28 Jan 2025

Medium riskHealth Canada

An official Health Canada notice concerns Medrad® centargo injection system. Centargo patient line sensor is a component of the Centargo injection system which detects a patient line. An investigation into reported air injection concerns found that, under certain special conditions, the patient line sensor may occasionally have difficulty detecting the presence of the patient line. This intermittent detection issue, combined with user reliance on automated system functions (such as auto-prime) and possible workflow inconsistencies, may slightly increase the likelihood of small air injections (1-10 ml). However, the overall risk remains low. Recall start date: December 13, 2024 Published 2025-01-28.

What to do now

Customers will be notified with instructions to follow.

Recall number

76870

Official notice

2025-01-28

The hazard

Centargo patient line sensor is a component of the Centargo injection system which detects a patient line. An investigation into reported air injection concerns found that, under certain special conditions, the patient line sensor may occasionally have difficulty detecting the presence of the patient line. This intermittent detection issue, combined with user reliance on automated system functions (such as auto-prime) and possible workflow inconsistencies, may slightly increase the likelihood of small air injections (1-10 ml). However, the overall risk remains low. Recall start date: December 13, 2024

How to check if you're affected

Compare the product name and identifiers below with the item you own. Follow the official notice if they match.

Recall Numbers

76870

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Affected products

Product 1

Affected products - MEDRAD® Centargo Injection System, Lot or serial number - Contact the manufacturer., Model or catalog number - CENT-SYS-BAT

Risk / hazard

Centargo patient line sensor is a component of the Centargo injection system which detects a patient line. An investigation into reported air injection concerns found that, under certain special conditions, the patient line sensor may occasionally have difficulty detecting the presence of the patient line. This intermittent detection issue, combined with user reliance on automated system functions (such as auto-prime) and possible workflow inconsistencies, may slightly increase the likelihood of small air injections (1-10 ml). However, the overall risk remains low. Recall start date: December 13, 2024

Where it was sold

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

Location 1

CA · Canada

Affected area 1

CA · Canada

Company & contacts

Manufacturer

Not provided

Phone

Not provided

Brand: Imaxeon, Medrad® Centargo Injection System.

Source & status

Source

Health Canada

Tier

official

Category

HEALTH

Classification

Type II

App estimate

medium

Recall details

Recall number

76870

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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