Hollister AnchorFast SlimFit, Oral Endotracheal Tube Fastener, REF 9787 recall — FDA Z-1179-2025
Hollister received reports of decreased skin barrier wear time which could can lead to tube migration
Overview of recall records associated with Hollister Inc., including dates, categories and classifications where available.
Classification mix: Class II: 5.
Hollister received reports of decreased skin barrier wear time which could can lead to tube migration
Hollister received reports of decreased skin barrier wear time which could can lead to tube migration
Hollister received reports of decreased skin barrier wear time which could can lead to tube migration
Hollister received reports of decreased skin barrier wear time which could can lead to tube migration
The tube holder can separate from the barrier that secures the device to the patients' body. The tube holder has the potential failure to separate from the barrier. This separation might…
This page summarizes recall records in which the official source identifies Hollister Inc. as the recalling firm or manufacturer. The number of records should not be treated as a safety rating or a measure of company size, because recall counts depend on product mix, reporting periods and how government records are organized.
Compare the dates, categories and classifications together rather than relying on the total alone. Open an individual record for the recalled product, reason, distribution details and current instructions available from the source.