Medline recalls Hudson RCI Medium Concentration Oxygen Masks due to tubing disconnecting during use, potentially causing shortness of breath and hypoxia. Affected models include 1041CE, HUD1035, HUD1042, HUD1930, and HUDRHO41U.
Firm received multiple complaints regarding tubing disconnecting from oxygen mask. If issue occurs during use, may lead to delay in patient care and patient may experience shortness of breath leading to hypoxia, which may require medical intervention to prevent further respiratory deterioration.
Medline is recalling several oxygen masks that may disconnect during use, risking shortness of breath and hypoxia. This could lead to medical intervention if the disconnection occurs while a patient is receiving oxygen.
The oxygen masks have tubing that can disconnect during use. If this happens while a patient is receiving oxygen, it may cause shortness of breath and hypoxia, requiring medical intervention to prevent respiratory issues.
Healthcare professionals using these oxygen masks in medical settings are most at risk, particularly during patient care where oxygen delivery is critical.
Check for model numbers: 1041CE, HUD1035, HUD1042, HUD1930, or HUDRHO41U. These masks were sold with specific lot numbers from 2024 to 2025.
Identify the model number on the mask to see if it matches the recalled items listed in the recall notice.
Reach out to Medline Industries for guidance on next steps if you have a recalled mask.
Medline received complaints that the tubing disconnects from the oxygen mask during use, which could cause shortness of breath and hypoxia in patients.
Affected models include 1041CE, HUD1035, HUD1042, HUD1930, and HUDRHO41U.
No, but you should check if your mask is affected and contact Medline for guidance if you have a recalled model.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-1035-2026 — Medline Medline Hello, I own a Medline that is covered by recall Z-1035-2026 from Medline. 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.
