Quick summary: TactiFlex™ Ablation Catheter, Sensor Enabled™. Date: 2025-09-17.
TactiFlex™ Ablation Catheter, Sensor Enabled™
2025-09-17
Recommended action: compare your product with the official notice and follow the instructions published by the official source.
Recall details
Quick summary: TactiFlex™ Ablation Catheter, Sensor Enabled™. Date: 2025-09-17.
Affected product details
Structured information extracted from the official recall notice. Confirm the identifiers and instructions in the original notice.
Affected products
Issue
Abbott is issuing this recall letter related to the TactiFlex™ Ablation Catheter, Sensor Enabled™. As part of their postmarket surveillance and monitoring processes, Abbott became aware of a limited number of tip detachment events during catheter removal from the packaging. Although the packaging has not changed since the introduction of the device (2022), improper removal from the packaging can result in tip damage. While most damaged tips (26 out of 29 instances) were detected prior to catheter insertion into patients, Abbott has experienced 3 recent instances where tips have detached and remained in the patient (incidence rate of <1:100,000). In all three (3) cases there were no further adverse outcomes reported to the patients. Abbott has made changes to the packaging tray design to help mitigate tip damage during catheter removal and has recently started to deploy the new packaging.
What you should do
- Contact the manufacturer if you require additional information.
Additional official information
Contains information licensed under the Open Government Licence – Canada. SafetyPulse is independent of the Government of Canada.
Frequently asked questions
Answers based on the official recall notice.
Product images
Official product images from Health Canada.
Starting...
Explore more
Related recalls
Similar recalls and safety notices.