Preformed AGT Oral Endotracheal Tube Murphy Eye, High Volume, Low Pressure Cuff, REF 111780075

Class I - Dangerous

What Should You Do?

  1. Check if you have this product:
    UDI/DI 14026704341112, Batch Numbers: 18FG21, 18FG31, 18GG19, 18HG23, 18HG30, 18IG16, 18IG30, 18JG35, 18KG19, 18KG41, 18LG18, 19AG03, 19BG04, 19BG19, 19CG03, 19CT36, 19DT34, 19FT37, 19GT65, 19HT55, 19IT01, 19IT19, 19JT38, 19LT21, 20AT26, 20BG11, 20CT12, 20DT22, 20ET04, 20ET49, 20FT65, KME20H0627, KME20K0991, KME20K3625, KME20L2680, KME21A1113, KME21A2088, KME21A3085, KME21B0714, KME21B2708, KME21C0596, KME21C1167, KME21L0761, KME21L0859, KME22A1383, KME22B2543, KME22B2906, KME22D0652, KME22D3251, KME22E1151, KME22E1506, KME22G0386, KME22G3151, KME22G3270, KME22H2700, KME22J0257, KME22J1105, KME22J1335, KME22K3101, KME22M1594
  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 111780075

Product Codes/Lot Numbers:

UDI/DI 14026704341112, Batch Numbers: 18FG21, 18FG31, 18GG19, 18HG23, 18HG30, 18IG16, 18IG30, 18JG35, 18KG19, 18KG41, 18LG18, 19AG03, 19BG04, 19BG19, 19CG03, 19CT36, 19DT34, 19FT37, 19GT65, 19HT55, 19IT01, 19IT19, 19JT38, 19LT21, 20AT26, 20BG11, 20CT12, 20DT22, 20ET04, 20ET49, 20FT65, KME20H0627, KME20K0991, KME20K3625, KME20L2680, KME21A1113, KME21A2088, KME21A3085, KME21B0714, KME21B2708, KME21C0596, KME21C1167, KME21L0761, KME21L0859, KME22A1383, KME22B2543, KME22B2906, KME22D0652, KME22D3251, KME22E1151, KME22E1506, KME22G0386, KME22G3151, KME22G3270, KME22H2700, KME22J0257, KME22J1105, KME22J1335, KME22K3101, KME22M1594

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: Z-1877-2023

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