Medline recalls Hudson RCI mBrace ET Tube Holder with potential cheek/upper lip injury from improper fit. Affected units have specific model numbers and were sold in 2019.
Complaint defects have been noted regarding the adhesive elements of the device and the frame of the holder putting additional pressure on the patient's cheekbones and upper lip which may cause dermal injury depending on the device positioning.
Medline is recalling Hudson RCI mBr: a tracheal tube holder that may cause cheek or upper lip injury if it presses too hard on the face. This risk happens when the device is not positioned correctly.
The device's adhesive and frame can put pressure on the patient's cheekbones and upper lip. If the device is not positioned correctly, this pressure may cause skin injuries like cuts or bruises.
Healthcare workers using this device for tracheal tube fixation in medical settings. Patients with tracheal tubes are most at risk due to the device's position on the face.
Check for model number DYNJMBRC4B on the device. This product was sold in 2019 with specific case and unit numbers listed in the recall notice.
Look for the model number DYNJMBRC4B on the device to confirm it is affected.
Reach out to Medline Industries for guidance on next steps if you have the affected model.
The recall states that improper positioning may cause cheek or upper lip injury, so it is not safe for use without proper checks.
Check for model number DYNJMBRC4B on the device. This product was sold in 2019 with specific case and unit numbers listed in the recall notice.
The recall does not specify a remedy, so contact Medline Industries for guidance on next steps.
We’ve drafted a message you can send Medline Industries to request your refund or repair — edit it as you like.
Subject: Recall Z-0698-2025 — Medline Industries Medline Industries Hello, I own a Medline Industries that is covered by recall Z-0698-2025 from Medline Industries. 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.
