Reported Feb 26, 2025 · Ongoing
AnchorFast SlimFit, Oral Endotracheal Tube Fastener, REF 9787,
Hollister Incorporated
Moderate riskThis product could cause temporary or reversible health problems — stop using it.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: Hollister Incorporated · 2000 Hollister Dr · Libertyville, IL · 60048-3781
Is this the product you have?
- AnchorFast SlimFit, Oral Endotracheal Tube Fastener, REF 9787,
- Lot codes and dates
- UDI/DI 00610075095834
- Lot Numbers
4L1724L182
- Amount recalled
- 45 box / 540 eaches
This recall covers 4 products
The agency filed one notice per product. You are reading one of them; the other 3 are below.
Where it was sold
- Nationwide
Why it was recalled
Hollister received reports of decreased skin barrier wear time which could can lead to tube migration
This product could cause temporary or reversible health problems — stop using it.
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