Medline Industries, LP is recalling 13,496 medical procedure convenience kits because they contain Mastisol Liquid Adhesive vials with defective tubing. The butyrate tubing in these adhesive vials can crack when activated, potentially causing leaks or preventing the adhesive from being applied correctly during surgical procedures. These kits were distributed nationwide across the United States and are used in a wide variety of medical settings, including surgical centers and hospitals.
If the tubing in the adhesive vial cracks during use, it may lead to the loss of sterile adhesive or the presence of plastic fragments, which could disrupt medical procedures or affect wound closure. No specific injuries have been reported in this data, but the defect was identified following complaints regarding the Mastisol component.
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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 ยท Raw API Response
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