🔍 RecallPedia

AnchorFast Guard, Oral Endotracheal Tube Fastener, REF 9800,

Class I - Dangerous
🏥 Medical Devices Recalled: December 23, 2024 Hollister Incorporated Other Medical Devices Nationwide

What Should You Do?

  1. Check if you have this product:
    UDI/DI 00610075186518, Lot Numbers: 4K162, 4K172, 4K182, 4K192, 4K202, 4K212, 4K222, 4K232, 4K252, 4K262, 4L012, 4L022, 4L032, 4L042, 4L052, 4L132.
  2. Do not eat it: Even if it looks and smells fine, do not consume this product.
  3. Throw it away or return it: You can return the product to the store for a full refund.
  4. Seek medical attention if needed: If you've consumed this product and feel unwell, contact your doctor immediately.
  5. Report problems: Report any issues to the FDA's Safety Reporting Portal.

⚠️ Emergency: If you experience severe symptoms after consuming this product, call 911 or Poison Control at 1-800-222-1222.

Recall Details

Company:
Hollister Incorporated
Reason for Recall:
Hollister received reports of decreased skin barrier wear time which could can lead to tube migration
Classification:
Class I - Dangerous

Dangerous or defective products that predictably could cause serious health problems or death.

Status:
ongoing

Product Information

Full Description:

AnchorFast Guard, Oral Endotracheal Tube Fastener, REF 9800,

Product Codes/Lot Numbers:

UDI/DI 00610075186518, Lot Numbers: 4K162, 4K172, 4K182, 4K192, 4K202, 4K212, 4K222, 4K232, 4K252, 4K262, 4L012, 4L022, 4L032, 4L042, 4L052, 4L132.

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: Z-1181-2025

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