Arrow International, LLC is recalling 1,650 catheter kits and needles because the liquid adhesive used to assemble the devices was incorrectly manufactured by a supplier. This defect could cause the device components to fail or detach during use. The recall affects various products, including radial artery catheterization kits, introducer needles, and central venous access kits sold directly to hospitals and clinics across nine states.
The incorrectly manufactured adhesive may lead to device failure, potentially causing leakage, component separation, or the introduction of foreign material into a patient's bloodstream during injection or aspiration procedures. While no injuries have been reported, such failures in a clinical setting could cause serious complications during surgery or emergency care.
Intended for injection or aspiration of fluids.
Permits access to peripheral arterial circulation.
Permits venous access and catheter introduction to central circulation.
Intended for administration of epidural anesthetic.
Antimicrobial surface to help protect against bloodstream infections.
Provides protection against catheter-related bloodstream infections.
Permits short-term venous access and catheter introduction.
Permits short-term venous access with antimicrobial technology.
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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