Teleflex Medical recalls Hudson RCI Comfort Flo humidification systems with specific lot numbers due to potential water flooding in high flow oxygen therapy.
There is the potential for water to flood the column and enter the circuit under circumstances where an abnormal pressure differential is created between the water bottle and the column during high flow oxygen therapy.
Teleflex Medical is recalling Hudson RCI Comfort Flo humidification systems with remote temperature ports. The risk is water flooding the system during high flow oxygen therapy, which could lead to electrical issues.
During high flow oxygen therapy, abnormal pressure changes between the water bottle and humidifier column can cause water to flood into the electrical circuit. This may lead to electrical malfunctions or damage.
Patients using oxygen therapy with the recalled humidification systems are most at risk. The affected units have specific lot numbers and model references.
Check for lot numbers starting with 74M, 74B, 74C, 74D, 74E, 74F, 74G, 74H, 74J, 74K, 74L, or 74M on the product label. The product includes a remote temperature port and humidifier nebulizer kit.
Look for lot numbers starting with 74M, 74B, 74C, 74D, 74E, 74F, 74G, 74H, 74J, 74K, or 74L on the product label.
Reach out to Teleflex Medical for further instructions on how to address the issue if you have the recalled product.
During high flow oxygen therapy, abnormal pressure changes between the water bottle and humidifier column can cause water to flood into the electrical circuit, potentially causing electrical malfunctions.
Check for lot numbers starting with 74M, 74B, 74C, 74D, 74E, 74F, 74G, 74H, 74J, 74K, or 74L on the product label. The product includes a remote temperature port and humidifier nebulizer kit.
Contact Teleflex Medical for further instructions on how to address the issue if you have the recalled product.
We’ve drafted a message you can send Teleflex Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-1115-2020 — Teleflex Medical Teleflex Medical Hello, I own a Teleflex Medical that is covered by recall Z-1115-2020 from Teleflex Medical. 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.
