🔍 RecallPedia

Preformed AGT Oral Endotracheal Tube Murphy Eye, High Volume, Low Pressure Cuff, REF 111780040

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 14026704341044, Batch Numbers: 18FG24, 18GG03, 18GG04, 18GG24, 18GT26, 18HG24, 18JG07, 18KG22, 18KG34, 18LG33, 19AG36, 19BG12, 19CG07, 19CT69, 19DT42, 19ET58, 19FT18, 19GT43, 19GT44, 19JT55, 19KT38, 19LT32, 20AT09, 20AT49, 20BT53, 20DT24, 20ET50, 20FT36, 20FT60, 20GT40, KME21C0405, KME21C1057, KME22C0550, KME22C0648, KME22C1816, KME22C2806, KME22D1073, KME22D2150, KME22E0683, KME22E0684, KME22E2814, KME22E2897, KME22F1760, KME22F2739, KME22G0790, KME22H1304, KME22H2878, KME22J1447, KME22K0482, KME23A1241, KME23A2001, KME23A2181, KME23A2683, KME23A3032
  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 111780040

Product Codes/Lot Numbers:

UDI/DI 14026704341044, Batch Numbers: 18FG24, 18GG03, 18GG04, 18GG24, 18GT26, 18HG24, 18JG07, 18KG22, 18KG34, 18LG33, 19AG36, 19BG12, 19CG07, 19CT69, 19DT42, 19ET58, 19FT18, 19GT43, 19GT44, 19JT55, 19KT38, 19LT32, 20AT09, 20AT49, 20BT53, 20DT24, 20ET50, 20FT36, 20FT60, 20GT40, KME21C0405, KME21C1057, KME22C0550, KME22C0648, KME22C1816, KME22C2806, KME22D1073, KME22D2150, KME22E0683, KME22E0684, KME22E2814, KME22E2897, KME22F1760, KME22F2739, KME22G0790, KME22H1304, KME22H2878, KME22J1447, KME22K0482, KME23A1241, KME23A2001, KME23A2181, KME23A2683, KME23A3032

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: Z-1941-2023

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