Reported Feb 26, 2025 · Ongoing

AnchorFast Guard Select, Oral Endotracheal Tube Fastener, REF 9700,

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 Select, Oral Endotracheal Tube Fastener, REF 9700,
Lot codes and dates
  • UDI/DI 00610075095810
  • Lot Numbers
    • 4J162
    • 4J172
    • 4J182
    • 4L172
    • 4L182
Amount recalled
701 box / 8,412 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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Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA device enforcement) notice

Data as of Sep 19, 7:47 PM UTC

RecallNow is not a government agency. Every fact on this page is published by the FDA, USDA or CPSC and links back to their notice.