Preformed AGT Oral Endotracheal Tube Murphy Eye, High Volume, Low Pressure Cuff, REF 111780035

Class I - Dangerous

What Should You Do?

  1. Check if you have this product:
    UDI/DI 14026704341037, Batch Numbers: 18GG03, 18GG24, 18GT26, 18HG36, 18IG11, 18JG07, 18JG14, 18JG36, 18KG22, 18KG34, 18LG31, 19AG21, 19AG36, 19BG12, 19CG07, 19CT36, 19CT69, 19DT42, 19FT22, 19FT49, 19GT43, 19HT03, 19JT01, 19JT20, 19JT55, 19LT32, 20AT09, 20CT24, 20DT15, 20ET04, 20ET56, 20GG43, 20GT18, KME20H2627, KME20L2489, KME20M0355, KME20M1519, KME21A0965, KME21A2395, KME21B1964, KME21B2528, KME21C0337, KME22A1674, KME22B1172, KME22B1719, KME22C0647, KME22D0114, KME22D2229, KME22E0680, KME22E1094, KME22E2895, KME22E2896, KME22F1454, KME22F1458, KME22F2737, KME22G0575, KME22H0031, KME22H0797, KME22H1789, KME22H2875, KME22H3073, KME22J1158, KME22J1777, KME22K2438, KME22L1579, KME22L1617, KME22L1659, KME22L1725, KME23A2277, KME23A3144, KME23B0437
  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 111780035

Product Codes/Lot Numbers:

UDI/DI 14026704341037, Batch Numbers: 18GG03, 18GG24, 18GT26, 18HG36, 18IG11, 18JG07, 18JG14, 18JG36, 18KG22, 18KG34, 18LG31, 19AG21, 19AG36, 19BG12, 19CG07, 19CT36, 19CT69, 19DT42, 19FT22, 19FT49, 19GT43, 19HT03, 19JT01, 19JT20, 19JT55, 19LT32, 20AT09, 20CT24, 20DT15, 20ET04, 20ET56, 20GG43, 20GT18, KME20H2627, KME20L2489, KME20M0355, KME20M1519, KME21A0965, KME21A2395, KME21B1964, KME21B2528, KME21C0337, KME22A1674, KME22B1172, KME22B1719, KME22C0647, KME22D0114, KME22D2229, KME22E0680, KME22E1094, KME22E2895, KME22E2896, KME22F1454, KME22F1458, KME22F2737, KME22G0575, KME22H0031, KME22H0797, KME22H1789, KME22H2875, KME22H3073, KME22J1158, KME22J1777, KME22K2438, KME22L1579, KME22L1617, KME22L1659, KME22L1725, KME23A2277, KME23A3144, KME23B0437

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: Z-1940-2023

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