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 device is used during medical procedures to hold breathing tubes in place.
The device's adhesive and frame can put pressure on the patient's cheekbones and upper lip. If the device is not positioned correctly, it may cause skin injuries like cuts or bruising.
Healthcare professionals using this device during medical procedures are most at risk. Patients receiving tracheal intubation may experience injury if the device is improperly positioned.
Look for the model number DYNJMBRC2B on the device. The product was sold in 2019 with specific case and unit numbers listed in the recall notice.
Verify the model number on the device is DYNJMBRC2B.
Reach out to Medline Industries for guidance on safe use or replacement.
The recall states it may cause dermal injury depending on device positioning, but does not specify serious injury risk.
Check for model number DYNJMBRC2B on the device. The product was sold in 2019 with specific case and unit numbers listed in the recall notice.
Contact Medline Industries for guidance on safe use or replacement options.
We’ve drafted a message you can send Medline Industries to request your refund or repair — edit it as you like.
Subject: Recall Z-0696-2025 — Medline Industries Medline Industries Hello, I own a Medline Industries that is covered by recall Z-0696-2025 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.
