Health product recall

HeartStart Intrepid Monitor/Defibrillator

Last updated

Summary

Product
HeartStart Intrepid Monitor/Defibrillator
Issue
Medical devices - Performance
What to do

Contact the manufacturer if you require additional information. 

Audience
Healthcare

Affected products

Affected products

Lot or serial number

Model or catalog number

HeartStart Intrepid Monitor/Defibrillator

All lots.

867172

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

Additional information

Details
Original published date:
Alert / recall type
Health product recall
Category
Health products - Medical devices - Cardiovascular
Companies

Philips Goldway (Shenzhen) Industrial Inc.

No.2 Keji North 3rd Road, Shenzhen, China, 518057

Published by
Health Canada
Audience
Healthcare
Recall class
Type II
Identification number
RA-74608

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