🔍 RecallPedia

Preformed AGT Oral Endotracheal Tube uncuffed/plain - Murphy, REF 100181030

Class I - Dangerous
🏥 Medical Devices Recalled: May 25, 2023 TELEFLEX Other Medical Devices Nationwide

What Should You Do?

  1. Check if you have this product:
    UDI/DI 14026704340528, Batch Numbers: 18GG23, 18HG17, 18HG21, 18IG17, 18LG18, 19AG25, 19BG19, 19BG32, 19GT16, 19IT53, 19LT21, KME22F2174, KME22G1753
  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:
TELEFLEX LLC
Reason for Recall:
Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.
Classification:
Class I - Dangerous

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

Status:
ongoing

Product Information

Full Description:

Preformed AGT Oral Endotracheal Tube uncuffed/plain - Murphy, REF 100181030

Product Codes/Lot Numbers:

UDI/DI 14026704340528, Batch Numbers: 18GG23, 18HG17, 18HG21, 18IG17, 18LG18, 19AG25, 19BG19, 19BG32, 19GT16, 19IT53, 19LT21, KME22F2174, KME22G1753

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: Z-1870-2023

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