Molded Products, Inc. is recalling approximately 26,900 units of its MPC-130 See Luer Cap Set. The recall was initiated after a confirmed complaint that the threaded sleeve of the device can fail to engage and become detached. If you use this device, please contact your healthcare provider or the manufacturer to arrange for a return or replacement.
The threaded sleeve on the cap set can become unattached or fail to engage properly, which can lead to the disconnection of intravascular administration sets. This poses a risk of treatment interruption or potential exposure to contaminants.
Recall Number: Z-1774-2026
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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