Medline Industries, LP is recalling approximately 3,491,866 units of Medline Sterile Water and Medline Sterile 0.9% Normal Saline (100mL) bottles, as well as various medical procedure kits containing these products. The recall was issued because the bottles may leak at the point where the foil seal meets the bottle opening, which could compromise the sterility of the fluid inside. No injuries or incidents have been reported in connection with this issue at this time.
A leaking seal can allow bacteria or other environmental contaminants to enter the bottle, making the liquid no longer sterile. Using non-sterile water or saline during medical procedures or wound care can lead to serious infections or other health complications for patients.
Recall #: Z-1705-2025
Recall #: Z-1706-2025
Recall #: Z-1707-2025
Recall #: Z-1708-2025
Recall #: Z-1709-2025
Recall #: Z-1709-2025
Recall #: Z-1709-2025
Recall #: Z-1709-2025
Recall #: Z-1709-2025
Recall #: Z-1709-2025
Recall #: Z-1710-2025
Recall #: Z-1711-2025
Recall #: Z-1711-2025
Recall #: Z-1712-2025
Recall #: Z-1713-2025
Recall #: Z-1714-2025
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
openFDA Disclaimer: This recall information is sourced from the openFDA API. Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Refer to the openFDA terms of service for more information.