Health product recall

Medtronic Restore™ Clinician Programmer Application

Brand(s)
Last updated

Summary

Product
Medtronic Restore™ Clinician Programmer Application
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
Restore™ Clinician Programmer Application More than 10 numbers, contact manufacturer. A71100

Issue

Medtronic is initiating a medical device recall (notification) to notify consignees of a potential for a software issue that may occur when attempting to clear a device reset message using the model A71100 Restore Clinician Programmer application (CP App). The A71100 CP App is used to program the restore family of Spinal Cord Stimulation implantable neurostimulators (INS).
A device reset can occur for a variety of reasons, including when the INS has an overdischarged battery, which is normally cleared during a programming session. In rare cases, the device reset message cannot be cleared and may result in the inability to resume therapy resulting in the patient experiencing a recurrence of underlying pain symptoms. Resolution would require surgical replacement of the INS to resume therapy.
 

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 II
Recall date
Identification number
RA-81294

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