Ct900 Clinician Programmer Software Application A710 Intellis & A810 Synchromed (2019-07-29)

Recall Summary Medtronic is recalling the CT900 Clinician Programmer Software Application for use with Intellis and Synchromed infusion pump systems in Canada due to a software issue that could affect device operation. This recall applies to healthcare facilities and clinicians who use this programming software across Canada. The Food and Drug Administration classified this as a Class I recall, indicating a serious potential health risk.

Reason

Medical devices

Classification

Class I

Category

drug recall

Country

Canada

Agency

HC-DEVICES

Recall date

2019-08-23

Status

Ongoing

Distribution

Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/000c8b0a-697d-4cee-9d63-306002bc2ff3