🔍 RecallPedia

AMT Male ENFit-to-Stepped Male (Christmas Tree) Adapter, Model Number ETRN102. Box PN TRN102, Box UDI (01)00842071109066(17)230901(10)200918-103, Pouch PN ETRN102, Pouch UDI (01)00842071108007(17)230901(10)200902-075

Class I - Dangerous
🏥 Medical Devices Recalled: November 10, 2020 Applied Medical Technology Other Medical Devices Nationwide

What Should You Do?

  1. Check if you have this product:
    Box Lot Number 200918-103; Pouch Lot Number 200902-075
  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:
The products subject to this recall may contain obvious, incorrect pouch labels while the outer box has the correct label.
Classification:
Class I - Dangerous

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

Status:
terminated

Product Information

Full Description:

AMT Male ENFit-to-Stepped Male (Christmas Tree) Adapter, Model Number ETRN102. Box PN TRN102, Box UDI (01)00842071109066(17)230901(10)200918-103, Pouch PN ETRN102, Pouch UDI (01)00842071108007(17)230901(10)200902-075

Product Codes/Lot Numbers:

Box Lot Number 200918-103; Pouch Lot Number 200902-075

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: Z-0698-2021

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