Ventec Life Systems is recalling 42 VOCSN V+Pro ventilators because they may not have been properly tested for high-pressure conditions during manufacturing. This defect can cause an internal oxygen leak, resulting in the patient receiving less oxygen than intended. Additionally, the leaked oxygen creates an oxygen-enriched environment inside or around the device, which significantly increases the risk of a fire. Consumers and healthcare providers should check their device serial numbers immediately and contact the manufacturer to arrange for a return or replacement.
A manufacturing defect may cause an oxygen leak that reduces the concentration of oxygen delivered to the patient and creates a highly flammable, oxygen-enriched environment that poses a severe fire hazard.
Package serial number may include a "P" at the end.
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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