Reported Feb 26, 2025 · Ongoing
AnchorFast, Oral Endotracheal Tube Fastener, REF 9799,
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, Oral Endotracheal Tube Fastener, REF 9799,
- Lot codes and dates
- UDI/DI 00610075129386
- Lot Numbers
83 of 83 codes
Lot4I1924I2024I2124I2224I2324I2424I2524I2624I2724I2824I2924I3024J0124J0224J0324J0424J0524J0624J0724J0824J0924J1024J1124J1224J1324J1424J1524J1624J2124J2224J2324J2424J2524J2624J2724J2824J2924J3024J3124K0124K0224K0324K0424K0524K0624K0724K0824K0924K1024K1124K1224K1324K1424K1524K1624K1724K1824K1924K202
- Amount recalled
- 30,527 box / 366,324 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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The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.
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