Public recall detail

TactiFlex™ Ablation Catheter, Sensor Enabled™

2025-09-17

medium
Recall Safety notice
Quick summary

Quick summary: TactiFlex™ Ablation Catheter, Sensor Enabled™. Date: 2025-09-17.

Recommended action

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.

Official details

Affected product details

Structured information extracted from the official recall notice. Confirm the identifiers and instructions in the original notice.

BrandABBOTT MEDICAL
ProductTactiFlex™ Ablation Catheter, Sensor Enabled™
IssueMedical devices - Labelling and packaging Medical devices - Performance
Recall classType II
IdentificationRA-78084

Affected products

ProductTactiFlex™ Ablation Catheter, Sensor Enabled™
LotMore than 10 numbers, contact manufacturer.
ModelA-TFSE-DF
Serial numberMore than 10 numbers, contact manufacturer.
DescriptionTactiFlex™ Ablation Catheter, Sensor Enabled™
ProductTactiFlex™ Ablation Catheter, Sensor Enabled™
LotMore than 10 numbers, contact manufacturer.
ModelA-TFSE-FJ
Serial numberMore than 10 numbers, contact manufacturer.
DescriptionTactiFlex™ Ablation Catheter, Sensor Enabled™
ProductTactiFlex™ Ablation Catheter, Sensor Enabled™
LotMore than 10 numbers, contact manufacturer.
ModelA-TFSE-D
Serial numberMore than 10 numbers, contact manufacturer.
DescriptionTactiFlex™ Ablation Catheter, Sensor Enabled™
ProductTactiFlex™ Ablation Catheter, Sensor Enabled™
LotMore than 10 numbers, contact manufacturer.
ModelA-TFSE-F
Serial numberMore than 10 numbers, contact manufacturer.
DescriptionTactiFlex™ Ablation Catheter, Sensor Enabled™
ProductTactiFlex™ Ablation Catheter, Sensor Enabled™
LotMore than 10 numbers, contact manufacturer.
ModelA-TFSE-DD
Serial numberMore than 10 numbers, contact manufacturer.
DescriptionTactiFlex™ Ablation Catheter, Sensor Enabled™

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
AudienceHealthcare
CategoryHealth products - Medical devices - Cardiovascular
CompaniesAbbott Medical 5050 Nathan Lane North, Plymouth, Minnesota, United States, 55442
Recall date2025-09-10
Published byHealth Canada
Recall classType II
Alert / recall typeHealth product recall
Identification numberRA-78084
Background{}
CompaniesAbbott Medical 5050 Nathan Lane North, Plymouth, Minnesota, United States, 55442
AudiencesHealthcare
Source updated2025-09-17

Contains information licensed under the Open Government Licence – Canada. SafetyPulse is independent of the Government of Canada.

Starting...

Related recalls

Similar recalls and safety notices.

Loading related recalls...