🔍 RecallPedia

Preformed AGT Oral Endotracheal Tube uncuffed/plain - Murphy, REF 100180070

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 14026704340511, Batch Numbers: 18HG40, 18LG33, 19CT36, 19FT19, 19GT46, 19LT31, KME21A2555, KME22H2313, KME22K1045
  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 100180070

Product Codes/Lot Numbers:

UDI/DI 14026704340511, Batch Numbers: 18HG40, 18LG33, 19CT36, 19FT19, 19GT46, 19LT31, KME21A2555, KME22H2313, KME22K1045

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: Z-1869-2023

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