Hollister recalls AnchorFast oral endotracheal tube fasteners with specific lot numbers due to potential tube migration from decreased skin barrier wear time.
Hollister received reports of decreased skin barrier wear time which could can lead to tube migration
Hollister is recalling certain AnchorFast oral endotracheal tube fasteners because they may cause the tube to migrate due to reduced skin barrier wear time. This could lead to breathing difficulties for patients using the device.
The fasteners have a decreased skin barrier wear time, which can cause the tube to migrate from the mouth. This migration could lead to breathing difficulties if the tube moves too far into the throat or airway.
Healthcare professionals who use the AnchorFast fasteners in medical settings are most at risk. Patients receiving endotracheal tube care with these specific models may be affected.
Check for the AnchorFast oral endotracheal tube fastener with lot numbers listed in the recall (e.g., 4I192, 4I202, up to 4K302). The product is sold under the reference number REF 9799.
Look for the lot numbers listed in the recall (e.g., 4I192, 4I202, 4I212, etc.) on the fastener packaging or label.
Reach out to Hollister Incorporated for further assistance or to confirm if your specific model is affected.
Hollister received reports that the AnchorFast fasteners may cause tube migration due to decreased skin barrier wear time.
Lot numbers 4I192 through 4K302 (as listed in the recall notice).
The recall does not specify a fix; users should check if their product is affected and contact Hollister for further guidance.
We’ve drafted a message you can send Hollister to request your refund or repair — edit it as you like.
Subject: Recall Z-1180-2025 — Hollister Hollister Hello, I own a Hollister that is covered by recall Z-1180-2025 from Hollister. 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.
