Hollister Incorporated Recalls
4 recalls from federal safety databases (FDA, CPSC). Sourced directly from government enforcement feeds.
Medical Device Recalls (4)
- Class II
December 23, 2024
AnchorFast SlimFit, Oral Endotracheal Tube Fastener, REF 9787,
Hollister received reports of decreased skin barrier wear time which could can lead to tube migration
- Class II
December 23, 2024
AnchorFast, Oral Endotracheal Tube Fastener, REF 9799,
Hollister received reports of decreased skin barrier wear time which could can lead to tube migration
- Class II
December 23, 2024
AnchorFast Guard Select, Oral Endotracheal Tube Fastener, REF 9700,
Hollister received reports of decreased skin barrier wear time which could can lead to tube migration
- Class II
December 23, 2024
AnchorFast Guard, Oral Endotracheal Tube Fastener, REF 9800,
Hollister received reports of decreased skin barrier wear time which could can lead to tube migration
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