Preformed AGT Oral Endotracheal Tube Murphy Eye, High Volume, Low Pressure Cuff, REF 111780055

Class I - Dangerous

What Should You Do?

  1. Check if you have this product:
    UDI/DI 14026704341075, Batch Numbers: 18FG23, 18FG24, 18GG03, 18GT26, 18IT05, 18IT06, 18JG36, 18KG08, 18KG34, 18KG44, 18LG11, 18LG31, 19AG21, 19AG36, 19CT36, 19DT06, 19FT18, 19HT80, 19LT04, 20AT09, 20AT49, 20DT14, 20FT59, 20FT60, KME20H2632, KME20J1207, KME20K0629, KME20K2746, KME20L0661, KME20L1622, KME20M0351, KME21A0978, KME21A2488, KME21B1917, KME21C1735, KME21E1424, KME22C0548, KME22C0549, KME22D0160, KME22D0263, KME22E1097, KME22F1274, KME22G0791, KME22H0940, KME22H2230, KME22H2331, KME22H3266, KME22J2275, KME22J2875, KME22K2770, KME23A0296, KME23A0482, KME23A0601, KME23A2865, KME23A3176
  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 111780055

Product Codes/Lot Numbers:

UDI/DI 14026704341075, Batch Numbers: 18FG23, 18FG24, 18GG03, 18GT26, 18IT05, 18IT06, 18JG36, 18KG08, 18KG34, 18KG44, 18LG11, 18LG31, 19AG21, 19AG36, 19CT36, 19DT06, 19FT18, 19HT80, 19LT04, 20AT09, 20AT49, 20DT14, 20FT59, 20FT60, KME20H2632, KME20J1207, KME20K0629, KME20K2746, KME20L0661, KME20L1622, KME20M0351, KME21A0978, KME21A2488, KME21B1917, KME21C1735, KME21E1424, KME22C0548, KME22C0549, KME22D0160, KME22D0263, KME22E1097, KME22F1274, KME22G0791, KME22H0940, KME22H2230, KME22H2331, KME22H3266, KME22J2275, KME22J2875, KME22K2770, KME23A0296, KME23A0482, KME23A0601, KME23A2865, KME23A3176

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: Z-1944-2023

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