B. Braun Medical Inc. has recalled approximately 93,390 units of various Perifix FX and Espocan Continuous Epidural Anesthesia Trays and Sets. The recall was issued because the lid of the catheter connector may be in the incorrect position, which can prevent a secure connection or cause medication to leak. These trays are clinical kits used in hospitals for delivering pain management through spinal or epidural anesthesia.
An improperly positioned connector lid can result in the catheter failing to connect properly, leading to leaks of anesthesia or medication errors. This interruption in delivery can result in inadequate pain management or require clinicians to perform additional procedures, posing a significant risk during surgery or labor.
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
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