Medline Industries, LP has recalled 50,271 medical kits containing Tego Connectors because the silicone seals on the connectors may tear or bulge (dome). This defect can block the flow of fluids, making it impossible for healthcare providers to inject or withdraw blood or medication through the connector. The affected kits include various dialysis, apheresis, and central line insertion trays and packs sold under the Medline and Centurion brands.
A damaged or torn seal can lead to fluid leakage, an interruption in critical therapy, or the accidental infusion of air or biological contaminants into a patient's body. These issues can result in serious medical complications or delays in necessary treatment.
Recall #: Z-1463-2026
Recall #: Z-1463-2026
Recall #: Z-1464-2026
Recall #: Z-1465-2026
Recall #: Z-1465-2026
Recall #: Z-1465-2026
Recall #: Z-1465-2026
Recall #: Z-1465-2026
Recall #: Z-1465-2026
Recall #: Z-1465-2026
Recall #: Z-1466-2026
Recall #: Z-1466-2026
Recall #: Z-1467-2026
Recall #: Z-1467-2026
Recall #: Z-1467-2026
Recall #: Z-1467-2026
Recall #: Z-1467-2026
Recall #: Z-1468-2026
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
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.