Health product recall

TactiFlex™ Ablation Catheter, Sensor Enabled™

Brand(s)
Last updated

Summary

Product
TactiFlex™ Ablation Catheter, Sensor Enabled™
Issue
Medical devices - Labelling and packaging
Medical devices - Performance
What to do

Contact the manufacturer if you require additional information. 

Audience
Healthcare

Affected products

Affected products Lot or serial number Model or catalogue number
TactiFlex™ Ablation Catheter, Sensor Enabled™ More than 10 numbers, contact manufacturer. A-TFSE-DF
TactiFlex™ Ablation Catheter, Sensor Enabled™ More than 10 numbers, contact manufacturer. A-TFSE-FJ
TactiFlex™ Ablation Catheter, Sensor Enabled™ More than 10 numbers, contact manufacturer. A-TFSE-D
TactiFlex™ Ablation Catheter, Sensor Enabled™ More than 10 numbers, contact manufacturer. A-TFSE-F
TactiFlex™ Ablation Catheter, Sensor Enabled™ More than 10 numbers, contact manufacturer. A-TFSE-DD

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.

Additional information

Details
Original published date:
Alert / recall type
Health product recall
Category
Health products - Medical devices - Cardiovascular
Companies
Abbott Medical
5050 Nathan Lane North, Plymouth, Minnesota, United States, 55442
Published by
Health Canada
Audience
Healthcare
Recall class
Type II
Recall date
Identification number
RA-78084

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