Reported Feb 26, 2025 · Ongoing
AnchorFast Guard, Oral Endotracheal Tube Fastener, REF 9800,
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 Guard, Oral Endotracheal Tube Fastener, REF 9800,
- Lot codes and dates
- UDI/DI 00610075186518
- Lot Numbers
4K1624K1724K1824K1924K2024K2124K2224K2324K2524K2624L0124L0224L0324L0424L0524L132
- Amount recalled
- 4,955 box / 59,460 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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