Medline Industries, LP has recalled 26,715 Adult Blood and Blood Culture Kits because some kits contain a Bactec component with an expiration date that does not match the information on the kit's outer insert. If a medical professional relies on the kit insert rather than checking the bottle itself, they may inadvertently use an expired component during blood collection or testing. These kits were distributed nationwide across the United States between December 2023 and early 2024.
Using an expired Bactec component can lead to inaccurate blood culture results, potentially causing delayed or incorrect treatment for serious infections. While no injuries have been reported, the risk remains that the chemical integrity of the component may be compromised after its true expiration date.
Contact healthcare provider or manufacturer for instructions.
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
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.