Medline Industries, LP is recalling 21,048 units of its Nexus 19/20G Catheter Connectors and various clinical procedure kits, including epidural, spinal, and nerve block trays. The catheter connectors may not be in the fully open position, which can prevent a catheter from being inserted as intended during medical procedures. While no injuries have been reported, this defect can lead to treatment delays or failures. These products were distributed nationwide in the U.S. and to several international locations, including Canada and the UAE.
The connector defect prevents medical professionals from properly inserting catheters. If a catheter cannot be placed, it can cause delays in patient care or procedural complications during anesthesia or nerve block administration.
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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.