HeartSine Technologies Ltd: HeartSine samaritan PAD (Public Access
Recall reason: Automated external defibrillators were shipped in their test configuration so there is a potential to have incorrect language, and CPR duration resulting in the device prompting users to perform CPR for 5-seconds, and it could analyze heart rhythm and instruct users to deliver a shock every 5-seconds if a shockable heart rhythm is detected, potentially leading to no therapy or delayed therapy.. Recalled by HeartSine Technologies Ltd. Distribution: Worldwide - US Nationwide distribution in the states of TX, CA, IL, CO, FL, NC, MI and the countries of Netherlands, Japan, New Zealand.. Classification (Class II — potential health risk). Affected lots/dates: Type/UDI-DI or GTIN/Se
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