🔍 RecallPedia

AMT Initial Placement Dilator Set. Used to place gastrostomy devices.

Class I - Dangerous
🏥 Medical Devices Recalled: May 14, 2024 Applied Medical Technology Other Medical Devices Nationwide

What Should You Do?

  1. Check if you have this product:
    Model No: IP-DIL; UDI-DI: 00842071131876; Lot number: 231218-242; Exp. Date: 2026-11-01.
  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:
Applied Medical Technology Inc
Reason for Recall:
Devices were labelled with the incorrect guidewire labelling.
Classification:
Class I - Dangerous

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

Status:
ongoing

Product Information

Full Description:

AMT Initial Placement Dilator Set. Used to place gastrostomy devices.

Product Codes/Lot Numbers:

Model No: IP-DIL; UDI-DI: 00842071131876; Lot number: 231218-242; Exp. Date: 2026-11-01.

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: Z-2238-2024

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