Jolife AB is recalling 5 units of LUCAS 2, 3, and 3.1 Chest Compression Systems because demonstration units were mistakenly provided to a customer. These units were not designed or validated for clinical use on patients, but they could potentially be used during an actual emergency. No injuries or incidents have been reported in connection with this issue.
Using a demonstration unit on a patient during cardiac arrest carries a risk of device failure or ineffective chest compressions, as these units may not meet clinical safety and performance standards. This could lead to a delay in treatment or unsuccessful resuscitation during a life-threatening event.
Demonstration unit potentially utilized for clinical use.
Demonstration units potentially utilized for clinical use.
Demonstration units potentially utilized for clinical use. One serial (3518D104) is noted as Scrapped.
If you or a family member were harmed by this recalled product, you may have legal rights. Consider consulting a consumer protection attorney to understand your options for compensation.
This is general information, not legal advice. Go Backs is not a law firm and does not provide legal services.
AI-Enhanced Content: The summary, action steps, and risk assessment on this page were generated by AI from official government recall data to improve readability. This is not legal or medical advice. Always refer to the official agency sources below for authoritative information.
Sources: FDA iRES · Raw API Response
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