HeartStart Intrepid Monitor/Defibrillator recall in Canada: Performance issue
In plain language
This recall involves the HeartStart Intrepid Monitor/Defibrillator sold in Canada. It's being recalled because it may display intermittent ECG waveforms when using 5-lead or 10-lead ECG cables. Healthcare professionals should contact the manufacturer for additional information.
What to do
- Contact the manufacturer if you require additional information.
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Affected products
HeartStart Intrepid Monitor/Defibrillator
Model: 867172
Lot: Not applicable
Why this matters
Performance issue with ECG monitoring
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: Not applicable
- 3
Check the model number
Model numbers are typically on the product label or packaging.
Affected models: 867172
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?
Performance issue with ECG monitoring
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?
Yes, there may be a health risk. Performance issue with ECG monitoring
When was this product recalled?
This product was recalled on July 22, 2024.
Is the Philips Goldway [Shenzhen] Industrial Inc. brand affected by this recall?
Yes, Philips Goldway [Shenzhen] Industrial Inc. products are affected by this recall. This recall involves the HeartStart Intrepid Monitor/Defibrillator sold in Canada. It's being recalled because it may display intermittent ECG waveforms when using 5-lead or 10-lead ECG cables. Healthcare professionals should contact the manufacturer for additional information.