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No image published for this recall

Pump, medfusion, model 4000

Official notice

23 Nov 2023

Last checked

23 Nov 2023

High riskHealth Canada

An official Health Canada notice concerns Pump, medfusion, model 4000. Smiths Medical identified legacy software anomalies which may occur in the Medfusion 4000 syringe infusion pumps. The legacy software anomalies were identified during a historical review of the risk evaluations conducted during the software development process. The historical review determined that some of the risk evaluations conducted in the past did not fully account for all the risks associated with the issues. After re-evaluating the patient risk, Smiths Medical determined that the issues identified were associated with sufficient patient risk that it is necessary to notify users, even if the remediation for an issue was available in previous software versions. Recall start date: November 7, 2023 Published 2023-11-23.

What to do now

Contact the manufacturer if you require additional information.

Recall number

74633

Official notice

2023-11-23

The hazard

Smiths Medical identified legacy software anomalies which may occur in the Medfusion 4000 syringe infusion pumps. The legacy software anomalies were identified during a historical review of the risk evaluations conducted during the software development process. The historical review determined that some of the risk evaluations conducted in the past did not fully account for all the risks associated with the issues. After re-evaluating the patient risk, Smiths Medical determined that the issues identified were associated with sufficient patient risk that it is necessary to notify users, even if the remediation for an issue was available in previous software versions. Recall start date: November 7, 2023

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

74633

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Affected products

Product 1

Affected products - Pump, Medfusion, Model 4000, Lot or serial number - Contact the manufacturer, Model or catalogue number - 4000-0101-249 4000-0101-50 4000-0105-51 4000-0106-01 4000-0106-00 4000-0100-50 4000-0101-51 4000-0100-249

Risk / hazard

Smiths Medical identified legacy software anomalies which may occur in the Medfusion 4000 syringe infusion pumps. The legacy software anomalies were identified during a historical review of the risk evaluations conducted during the software development process. The historical review determined that some of the risk evaluations conducted in the past did not fully account for all the risks associated with the issues. After re-evaluating the patient risk, Smiths Medical determined that the issues identified were associated with sufficient patient risk that it is necessary to notify users, even if the remediation for an issue was available in previous software versions. Recall start date: November 7, 2023

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: Smiths Medical Asd, Pump Medfusion Model 4000.

Source & status

Source

Health Canada

Tier

official

Category

HEALTH

Classification

Type I

App estimate

high

Recall details

Recall number

74633

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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