CardioLab System - Amplifier recall in Canada: electrical shock risk
In plain language
This recall involves certain CardioLab System - Amplifiers sold in Canada. It's being recalled because some units failed a patient leakage current test, which could pose an electrical shock risk. Stop using the product and follow the return/repair steps in the official notice.
What to do
- Stop using the product immediately.
- Check the model and serial numbers.
- Contact GE Healthcare for instructions on return or repair.
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Affected products
CardioLab System - Amplifier
Model: 2088700-004
Lot: RXJ19224001TA
Why this matters
Electrical shock risk
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: RXJ19224001TA
- 3
Check the model number
Model numbers are typically on the product label or packaging.
Affected models: 2088700-004
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?
Electrical shock risk
What should consumers do?
Stop using the product immediately. Check the model and serial numbers. Contact GE Healthcare for instructions on return or repair.
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. Electrical shock risk
When was this product recalled?
This product was recalled on May 8, 2020.
Is the CardioLab System brand affected by this recall?
Yes, CardioLab System products are affected by this recall. This recall involves certain CardioLab System - Amplifiers sold in Canada. It's being recalled because some units failed a patient leakage current test, which could pose an electrical shock risk. Stop using the product and follow the return/repair steps in the official notice.