Seatex LLC is recalling 3,489 cases of 7-Eleven and PROBLEND hand sanitizers because an FDA inspection identified significant manufacturing deficiencies at their facility. The recall includes various gel and foaming hand sanitizers containing ethanol or benzalkonium chloride that were produced under conditions that deviated from Good Manufacturing Practice (CGMP) standards. No injuries or adverse reactions have been reported, but the products may not meet the quality and safety standards required by the FDA.
Manufacturing deficiencies can result in products that are ineffective or potentially contaminated with harmful substances. While no specific contaminants have been identified in this recall, products manufactured under poor quality control pose a risk to consumers who rely on them for infection prevention.
You have 2 options:
Recall #: D-0359-2024; Distributed by Magnus.
Recall #: D-0360-2024.
Recall #: D-0358-2024; Distributed by Magnus.
Recall #: D-0356-2024.
Recall #: D-0357-2024.
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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