Public recall detail

HeartStart Intrepid Monitor/Defibrillator

2023-11-17

medium
Recall Safety notice
Quick summary

Quick summary: HeartStart Intrepid Monitor/Defibrillator. Date: 2023-11-17.

Recommended action

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.

Official details

Affected product details

Structured information extracted from the official recall notice. Confirm the identifiers and instructions in the original notice.

BrandPhilips Goldway [Shenzhen] Industrial Inc.
ProductHeartStart Intrepid Monitor/Defibrillator
IssueMedical devices - Performance
Recall classType II
IdentificationRA-74608

Affected products

ProductHeartStart Intrepid Monitor/Defibrillator
LotAll lots.
Model867172
Serial numberAll lots.
DescriptionHeartStart Intrepid Monitor/Defibrillator

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
AudienceHealthcare
CategoryHealth products - Medical devices - Cardiovascular
CompaniesPhilips Goldway (Shenzhen) Industrial Inc. No.2 Keji North 3rd Road, Shenzhen, China, 518057
Published byHealth Canada
Recall classType II
Alert / recall typeHealth product recall
Identification numberRA-74608
Background{}
CompaniesPhilips Goldway (Shenzhen) Industrial Inc. No.2 Keji North 3rd Road, Shenzhen, China, 518057
AudiencesHealthcare
Source updated2023-11-17

Contains information licensed under the Open Government Licence – Canada. SafetyPulse is independent of the Government of Canada.

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