CardioMEMS recall in Canada: System error
In plain language
This recall involves the CardioMEMS Patient and Hospital Electronics System sold in Canada. It's being recalled because some units may show a false system error message. Stop using the product and follow the return/repair steps in the official notice.
What to do
- Stop using the product immediately.
- Check model and serial numbers.
- Contact St. Jude Medical for instructions.
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Affected products
CardioMEMS Patient Electronics System
Model: CM1100
Lot: P180107823
CardioMEMS Hospital Electronics System
Model: CM3000
Lot: M171108427
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: M171108427, P180107823
- 3
Check the model number
Model numbers are typically on the product label or packaging.
Affected models: CM1100, CM3000
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 the CardioMEMS Patient and Hospital Electronics System sold in Canada. It's being recalled because some units may show a false system error message. Stop using the product and follow the return/repair steps in the official notice.
What should consumers do?
Stop using the product immediately. Check model and serial numbers. Contact St. Jude Medical for instructions.
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 June 29, 2018.
Is the CardioMEMS brand affected by this recall?
Yes, CardioMEMS products are affected by this recall. This recall involves the CardioMEMS Patient and Hospital Electronics System sold in Canada. It's being recalled because some units may show a false system error message. Stop using the product and follow the return/repair steps in the official notice.