C.R. Bard Inc. is recalling 644,496 units of Bard Nasogastric Sump Tubes and related ENFit components, including Lopez Valves and Anti-Reflux Filters, because the devices may fail to provide adequate suction or drainage. The company has received multiple user complaints indicating that the tubes are not properly decompressing or draining during medical use. This defect could lead to patient discomfort or a failure to properly manage gastric fluids. Consumers and healthcare providers should check their inventory for the specific REF and lot numbers listed and contact the manufacturer for further guidance.
The affected tubes and connectors can experience inadequate or reduced suction and drainage, which prevents the medical device from properly clearing fluids or gases from a patient's stomach. This failure can delay necessary medical treatment or result in ineffective gastric decompression.
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 · Raw API Response
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