Preformed AGT Oral Endotracheal Tube Murphy Eye, High Volume, Low Pressure Cuff, REF 111781080

Class I - Dangerous

What Should You Do?

  1. Check if you have this product:
    UDI/DI 14026704341242, Batch Numbers: 18GG18, 18HG21, 18IG16, 18KG01, 18KG19, 18LG18, 19BG18, 19BG33, 19GT13, 19HT31, 19HT55, 19IT15, 19JT35, 19KT14, 19LT21, 20AT26, 20CT11, 20FT68, 20GT49, KME20M0409, KME21A1111, KME21A2095, KME21B2212, KME21C2483, KME21C3405, KME22B0921, KME22B0923, KME22D0289, KME22D1811, KME22D1855, KME22D2401, KME22E2898, KME22H2600, KME22H3295, KME22J2877, KME22K2861, KME22K3117, KME22M1510, KME22M2546, KME23B0521, KME23B3047
  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 Murphy Eye, High Volume, Low Pressure Cuff, REF 111781080

Product Codes/Lot Numbers:

UDI/DI 14026704341242, Batch Numbers: 18GG18, 18HG21, 18IG16, 18KG01, 18KG19, 18LG18, 19BG18, 19BG33, 19GT13, 19HT31, 19HT55, 19IT15, 19JT35, 19KT14, 19LT21, 20AT26, 20CT11, 20FT68, 20GT49, KME20M0409, KME21A1111, KME21A2095, KME21B2212, KME21C2483, KME21C3405, KME22B0921, KME22B0923, KME22D0289, KME22D1811, KME22D1855, KME22D2401, KME22E2898, KME22H2600, KME22H3295, KME22J2877, KME22K2861, KME22K3117, KME22M1510, KME22M2546, KME23B0521, KME23B3047

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: Z-1957-2023

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