Health product recall

Sphere-9™ Catheter

Brand(s)
Last updated

Summary

Product
Sphere-9™ Catheter
Issue
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
Sphere-9™ Catheter All lots. AFR-00001

Issue

There have been forty-six (46) reported incident reports (none of which were from Canada) where patients with a Biotronik ICD experienced induced ventricular arrhythmia (VT and/or VF) following RF ablation of cardiac tissue using the Affera Sphere-9 catheter.

Sphere-9 presents a higher current flow to the ICD or CRT-D which interacts with a safety feature built into Biotronik ICDs and CRT-Ds. The higher currents of the Sphere-9 catheter during RF application proceed to an unfavorable modulation of the coupled currents (approx. 40Hz frequency) that may be conducted via the implanted leads, and result in possible VT or VF induction.
 

Additional information

Details
Original published date:
Alert / recall type
Health product recall
Category
Health products - Medical devices - Cardiovascular
Companies

Medtronic Inc.

710 Medtronic Parkway N.E., Minneapolis, Minnesota, United States, 55432

Published by
Health Canada
Audience
Healthcare
Recall class
Type I
Recall date
Identification number
RA-82409

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