Cardinal Health recalls 4 models of Salem Sump Dual Lumen Stomach Tubes due to reported Anti-Reflux Valve breakage from improper use. No immediate action needed but label changes were made.
The firm received reports of breakage in the Anti-Reflux Valve (ARV) due to improper use. As a result, changes to labeling were made.
Cardinal Health is recalling four models of Salem Sump Dual Lumen Stomach Tubes after reports of Anti-Reflux Valve breakage due to improper use. This could lead to complications if the tube is not used correctly.
The Anti-Reflux Valve (ARV) in the tube can break if used improperly, potentially causing leaks or complications. This issue was reported by the manufacturer but does not indicate a high risk in normal use.
Patients using these stomach tubes for medical purposes are most at risk. Healthcare providers and caregivers who handle the tubes may also be affected.
Check for the model numbers 8888264929, 8888264945, 8888264960, or 8888264986 on the tube packaging. These are sterile stomach tubes sold by Cardinal Health.
Look for the model numbers 8888264929, 8888264945, 8888264960, or 8888264986 on the tube packaging.
Cardinal Health received reports of Anti-Reflux Valve breakage due to improper use, so they made label changes to address the issue.
No immediate action is needed, but ensure you follow proper usage guidelines to prevent valve breakage.
Check the model number on the tube packaging to see if it is affected. If it is, contact Cardinal Health for label changes.
We’ve drafted a message you can send Cardinal Health to request your refund or repair — edit it as you like.
Subject: Recall Z-3301-2024 — Cardinal Health Cardinal Health Hello, I own a Cardinal Health that is covered by recall Z-3301-2024 from Cardinal Health. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
