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Official recall record

AnchorFast Oral Endotracheal Tube Fastener

Health Canada — Medical Devices · 2025-01-03 · CanadaType II
Issuing authority
Health Canada — Medical Devices
Published
2025-01-03
Country of alert
Canada
Alert level
Type II
Alert type
recall

What the authority reported

Type II recall: This product is intended to provide a convenient means to hold an oral endotracheal tube securely in place without the use of adhesive tape. The oral endotracheal tube fastener allows repositioning of the tube in either direction along the track without removal of the device. Hollister is voluntarily recalling this product due to reports of decreased skin barrier pad wear time. Hollister has received 2 reports that this issue could lead to tube migration and clinical intervention in the USA. Recall Start Date: December 20, 2024

What to do

Follow the instructions in the official notice — recall remedies (refund, repair, replacement, or disposal) are defined by the issuing authority and the responsible business, and they differ per recall. Do not rely on summaries, including this one.

Verify at the source: Health Canada — Medical Devices — official record →
Record last checked against the registry on 2026-05-31.

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