Medtronic ICDs and CRT-Ds recall in Canada: software defect
In plain language
This recall involves Medtronic Implantable Cardioverter Defibrillators (ICDs) and Cardiac Resynchronization Therapy Defibrillators (CRT-Ds) sold in Canada. They are being recalled because of a software defect that may cause a telemetry error. Contact the manufacturer for more information.
What to do
- Contact the manufacturer if you require additional information.
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Affected products
Cobalt Vr Mri Surescan
Model: DVPB3D1, DVPB3D4
Lot: RSF604533S, RSF604560S, RSF604562S
Cobalt Dr Mri Surescan
Model: DDPB3D1, DDPB3D4
Lot: RSO606773S, RSO606771S, RSO606769S
Crome Dr Mri Surescan
Model: DDPC3D1, DDPC3D4
Carelink Smartsync Cobalt Crome Application
Model: D00U005
Crome Hf Quad Crt-D Mri Surescan
Model: DTPC2Q1, DTPC2QQ
Cobalt Hf Crt-D Mri Surescan
Model: DTPB2D1, DTPB2D4
Crome Hf Crt-D Mri Surescan
Model: DTPC2D1, DTPC2D4
Crome Vr Mri Surescan
Model: DVPC3D1, DVPC3D4
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: RSF604533S, RSF604560S, RSF604562S, RSO606773S, RSO606771S, RSO606769S
- 3
Check the model number
Model numbers are typically on the product label or packaging.
Affected models: D00U005, DDPB3D1, DDPB3D4, DDPC3D1, DDPC3D4, DTPB2D1, DTPB2D4, DTPC2D1, DTPC2D4, DTPC2Q1, DTPC2QQ, DVPB3D1, DVPB3D4, DVPC3D1, DVPC3D4
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?
This recall involves Medtronic Implantable Cardioverter Defibrillators (ICDs) and Cardiac Resynchronization Therapy Defibrillators (CRT-Ds) sold in Canada. They are being recalled because of a software defect that may cause a telemetry error. Contact the manufacturer for more information.
What should consumers do?
Contact the manufacturer if you require additional information.
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?
A potential safety risk has been identified with this product. Stop using it immediately and follow the instructions in the official recall notice.
When was this product recalled?
This product was recalled on May 9, 2022.
Is the MEDTRONIC INC. brand affected by this recall?
Yes, MEDTRONIC INC. products are affected by this recall. This recall involves Medtronic Implantable Cardioverter Defibrillators (ICDs) and Cardiac Resynchronization Therapy Defibrillators (CRT-Ds) sold in Canada. They are being recalled because of a software defect that may cause a telemetry error. Contact the manufacturer for more information.