Health product recall

Clinician Programmer for Vercise™ Deep Brain Stimulation (DBS) systems

Last updated

Summary

Product
Clinician Programmer for Vercise™ Deep Brain Stimulation (DBS) systems
Issue
Medical devices - Labelling and packaging
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

Clinician Programmer

More than 10 numbers, contact manufacturer.

DB-7164

Clinician Programmer

More than 10 numbers, contact manufacturer.

DB-7174

Vercise™ Clinician Programmer

More than 10 numbers, contact manufacturer.

DB-7164

Vercise™ Clinician Programmer

More than 10 numbers, contact manufacturer.

DB-7161

Vercise™ Clinician Programmer

More than 10 numbers, contact manufacturer.

DB-7174

Vercise™ DBS Clinician Programmer

More than 10 numbers, contact manufacturer.

DB-7164

Vercise™ DBS Clinician Programmer

More than 10 numbers, contact manufacturer.

DB-7161

Vercise™ DBS Clinician Programmer

More than 10 numbers, contact manufacturer.

DB-7174

Issue

Boston Scientific is initiating a Product Correction (IFU update) to provide additional guidance in the use of the Clinician Programmer feature for Implantable Pulse Generator (IPG) battery recharge interval and non-rechargeable IPG battery longevity estimates.

Additional information

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

Boston Scientific Neuromodulation Corporation

25155 Rye Canyon Loop, Valencia, California, United States, 91355

Published by
Health Canada
Audience
Healthcare
Recall class
Type II
Recall date
Identification number
RA-82953

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