Quick summary: HeartStart Intrepid Monitor/Defibrillator. Date: 2023-11-17.
HeartStart Intrepid Monitor/Defibrillator
2023-11-17
Recommended action: compare your product with the official notice and follow the instructions published by the official source.
Recall details
Quick summary: HeartStart Intrepid Monitor/Defibrillator. Date: 2023-11-17.
Affected product details
Structured information extracted from the official recall notice. Confirm the identifiers and instructions in the original notice.
Affected products
Issue
Philips has identified a potential safety and compliance issue: the HeartStart Intrepid Monitor/Defibrillator's service manual does not detail electrical safety test verification methods as required by International Electrotechnical Commission(IEC) requirements for class I devices. The current HeartStart Intrepid service manual does not detail IEC class I electrical safety test verification methods. The lack of this testing does not introduce a failure, but it may prevent a failure from being detected. This could occur when an IEC class I device is tested as a class II device after a servicing event. The issue was identified as the result of a service provider's inquiry. There have been no reports of patient harm. Recall start date: October 19, 2023
What you should do
- Contact the manufacturer if you require additional information.
Additional official information
Contains information licensed under the Open Government Licence – Canada. SafetyPulse is independent of the Government of Canada.
Frequently asked questions
Answers based on the official recall notice.
Product images
Official product images from Health Canada.
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