Cardinal Health recalls Salem Sump PVC gastroduodenal 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 tubes because users have reported Anti-Reflux Valve breakage when too much force is applied. This could lead to tube disconnection or other complications during medical procedures.
The Anti-Reflux Valve (ARV) in these tubes can break if excessive force is applied during use. This breakage may cause the tube to disconnect, leading to potential complications such as leaks or improper function during medical procedures.
Medical professionals using these tubes for procedures like gastric feeding or intestinal access are most at risk. Patients receiving these tubes through medical care are also affected.
Check for product codes like 1180264408, 1180264416, or 8888264804 on the tube packaging. These tubes are used in medical settings for gastric feeding or intestinal access procedures.
Inspect the tube for any signs of Anti-Reflux Valve damage or breakage before use.
Apply gentle force when handling the tube to avoid excessive pressure that could cause ARV breakage.
Cardinal Health has received complaints about Anti-Reflux Valve breakage due to excessive force during use.
Affected models include Salem Sump PVC Gastroduodenal Tubes with sizes like 10 Fr/Ch (3.3 mm) x 90 cm, 12 Fr/Ch (4.0 mm) x 114 cm, and others listed in the product codes.
No, but you should check for ARV breakage and use the tubes with care to avoid excessive force.
We’ve drafted a message you can send Cardinal Health to request your refund or repair — edit it as you like.
Subject: Recall Z-0211-2026 — Cardinal Health Cardinal Health Hello, I own a Cardinal Health that is covered by recall Z-0211-2026 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.
