Cardinal Health recalls Salem Sump PVC stomach tubes due to reported Anti-Reflux Valve breakage from excessive force during use. Affected models include various sizes and lengths.
Firm has received complaints regarding Anti-Reflux Valve (ARV) breakage due to excessive force during use. Firm is providing additional guidance for use. Expansion of RES 95214.
Cardinal Health is recalling Salem Sump PVC stomach tubes because users have reported Anti-Reflux Valve breakage when too much force is applied. This could lead to stomach contents flowing back into the esophagus, causing discomfort or infection.
The Anti-Reflux Valve (ARV) in these tubes can break if excessive force is applied during use. This breakage may allow stomach contents to flow back into the esophagus, potentially causing discomfort, infection, or other complications.
Patients using Salem Sump stomach tubes for medical purposes are most at risk. The product is used in hospitals and clinics for temporary digestive support.
Check for product codes including 264929, 264945, 264960, 264986, 5558264957, 5558264965, 5558264973, 5558264981, 8888264911, or 8888268060. These tubes were sold with various sizes and lengths.
Look for specific product codes listed in the recall notice to confirm if your tube is affected.
Reach out to Cardinal Health 200, LLC for further guidance on handling the recalled tubes.
The recall is due to reported Anti-Reflux Valve breakage from excessive force during use, which could lead to stomach contents flowing back into the esophagus.
Affected models include Salem Sump Stomach Tubes with product codes 264929, 264945, 264960, 264986, 5558264957, 5558264965, 5558264973, 5558264981, 8888264911, and 8888268060.
No, but you should check if your tube is affected and contact Cardinal Health 200, LLC for specific guidance.
We’ve drafted a message you can send Salem Sump to request your refund or repair — edit it as you like.
Subject: Recall Z-0207-2026 — Salem Sump Salem Sump Hello, I own a Salem Sump that is covered by recall Z-0207-2026 from Salem Sump. 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.
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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.
