Recall Z-1179-2025— Hollister Incorporated
Class II · Ongoing
Class II FDA medical device recall by Hollister Incorporated, initiated 2024-12-23. FDA's recall record names no specific 510(k) clearance for this event. Product: AnchorFast SlimFit, Oral Endotracheal Tube Fastener, REF 9787,. Reason: Hollister received reports of decreased skin barrier wear time which could can lead to tube migration.
- Recalling firm
- Hollister Incorporated
- Classification
- Class II
- Status
- Ongoing
- Initiated
- 2024-12-23
- Firm location
- Libertyville, IL, United States
Product description
AnchorFast SlimFit, Oral Endotracheal Tube Fastener, REF 9787,
Reason for recall
Hollister received reports of decreased skin barrier wear time which could can lead to tube migration
Data sourced from openFDA. This site is unofficial and independent of the FDA.