B Braun Medical Inc. is recalling 28,200 units of its Introcan Safety 3 Closed IV Catheter due to a manufacturing defect where the valve housing may detach. This defect leads to fluid leakage during use, which can interrupt medical procedures or expose caregivers to fluids. The recall specifically affects the 22 Ga. x 1 in. Purple Winged model (Model 4251128-02) from lot 24F09G8952.
The valve housing can detach from the catheter body, resulting in leakage of blood or medication. While no injuries have been reported, this failure can delay necessary medical treatment or increase the risk of healthcare worker exposure to patient blood.
Manufacturer return and correction
Passive safety IV catheter.
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.