Cardinal Health recalls Salem Sump PVC tubes due to reported Anti-Reflux Valve breakage from excessive force during use. Consumers should check product codes and follow safety guidelines to prevent injury.
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 the Anti-Reflux Valve breaking when too much force is applied. This could lead to leaks or other issues if the valve fails during use.
The Anti-Reflux Valve in Salem Sump tubes can break if excessive force is applied during use. This breakage may cause leaks or other issues, but the risk is not severe enough to cause serious injury in normal use.
Users of Salem Sump PVC tubes for medical or home use who have the product code 266197 are affected. Those using the tubes with high force or in situations where the valve might be stressed are at slightly higher risk.
Check for product code 266197 on the Salem Sump PVC tubes. The tubes are CE marked and sold with specific model numbers like 8888266197 and 10884527022762.
Look for product code 266197 on the Salem Sump PVC tubes to confirm if they are recalled.
Cardinal Health has received complaints about Anti-Reflux Valve breakage due to excessive force during use.
Check for product code 266197 on the Salem Sump PVC tubes, which are CE marked with model numbers like 8888266197.
The recall does not specify a remedy, so check with Cardinal Health for guidance on safe use or disposal.
We’ve drafted a message you can send Cardinal Health to request your refund or repair — edit it as you like.
Subject: Recall Z-0209-2026 — Cardinal Health Cardinal Health Hello, I own a Cardinal Health that is covered by recall Z-0209-2026 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.
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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.
