Medtronic Restore™ Clinician Programmer Application
In plain language
This recall involves the Medtronic Restore™ Clinician Programmer Application (model A71100) used to program spinal cord stimulators. It's being recalled because a software issue may prevent clearing a device reset message, which could lead to therapy interruption. This could result in a recurrence of pain symptoms, potentially requiring surgery to replace the device.
What to do
- Contact the manufacturer if you require additional information.
- This recall is primarily for healthcare professionals.
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Affected products
Restore™ Clinician Programmer Application
Model: A71100
Lot: More than 10 numbers, contact manufacturer.
Why this matters
Interruption of therapy, recurrence of pain symptoms, potential need for surgery
Do I have this product?
This recall only applies to specific products. Follow the steps below to check.
- 1
Check the product name
Make sure your product name matches one of the affected products listed above.
- 2
Check the lot number
Lot numbers identify specific production batches.
Affected lots: More than 10 numbers, contact manufacturer.
- 3
Check the model number
Model numbers are typically on the product label or packaging.
Affected models: A71100
If your product matches one or more of the details above, it may be affected by this recall.
If your product does not match these details, it is not affected by this recall.
When in doubt, always check the official notice.
Frequently Asked Questions
Why was this product recalled?
Interruption of therapy, recurrence of pain symptoms, potential need for surgery
What should consumers do?
Contact the manufacturer if you require additional information. This recall is primarily for healthcare professionals.
Where was the product sold?
This product was sold in Canada. For specific retailers or distribution areas, please check the official recall notice linked on this page.
Is there a health risk?
Yes, there may be a health risk. Interruption of therapy, recurrence of pain symptoms, potential need for surgery
When was this product recalled?
This product was recalled on November 28, 2025.
Is the MEDTRONIC INC. brand affected by this recall?
Yes, MEDTRONIC INC. products are affected by this recall. This recall involves the Medtronic Restore™ Clinician Programmer Application (model A71100) used to program spinal cord stimulators. It's being recalled because a software issue may prevent clearing a device reset message, which could lead to therapy interruption. This could result in a recurrence of pain symptoms, potentially requiring surgery to replace the device.