Endotracheal Tube oral/nasal Murphy Eye, High Volume, Low Pressure Cuff, REF 112082080

Class I - Dangerous

What Should You Do?

  1. Check if you have this product:
    UDI/DI 14026704341440, Batch Numbers: 18GG11, 18GG12, 18GG13, 18GT08, 18GT11, 18HG40, 18IG04, 18IG07, 18IG12, 18IG13, 18IG23, 18IT06, 18IT10, 18IT16, 18JG07, 18JG09, 18JG13, 18JG26, 18JG37, 18JG38, 18JT06, 18JT10, 19AG35, 19AG38, 19AT20, 19BG06, 19BG07, 19BG14, 19BG18, 19BG22, 19BG25, 19BG30, 19BT08, 19BT12, 19DT36, 19DT43, 19ET22, 19ET27, 19ET82, 19ET83, 19FT04, 19FT13, 19FT26, 19FT28, 19KT14, 19LT46, 19LT47, 19LT51, 20AT22, 20AT49, 20BG15, 20BG19, 20BT05, 20BT09, 20BT10, 20BT24, 20CT42, 20CT48, 20CT54, 20DT10, 20DT23, 20DT28, 20ET16, 20ET17, 20ET39, 20FT17, 20FT43, 20FT49, 20FT58, 20FT61, 20GG48, 20GT10, 20GT11, 20GT12, 20GT23, KME20G0436, KME20H0953, KME20L1706, KME20L2207, KME20L2333, KME20L2607, KME20L2696, KME20M1043, KME20M1342, KME21A1435, KME21A1524, KME21A2058, KME21B0616, KME21D1653, KME21D1946, KME21D2011, KME21D2012, KME21E0584, KME21E0687, KME21E1452, KME21F0981, KME21F1006, KME21F1215, KME21F1530, KME21F1604, KME21G0736, KME21G1100, KME21J0109, KME21J0563, KME21J1295, KME21J1364, KME21J1415, KME21J1532, KME21J2055, KME21K0022, KME21K0187, KME21K0449, KME21K2884, KME21K3013, KME21L0744, KME21L1438, KME21L1533, KME21L1661, KME21L1787, KME21L2012, KME21L2177, KME21M3032, KME21M3137, KME21M3236, KME22A0626, KME22A0793, KME22A1043, KME22A1701, KME22A2203, KME22A2429, KME22A2693, KME22A2966, KME22B0500, KME22B0737, KME22B0898, KME22B0915, KME22B0991, KME22C1987, KME22C2072, KME22C2219, KME22C2400, KME22C3376, KME22D0004, KME22D1589, KME22D1689, KME22D1897, KME22D2014, KME22D2505, KME22D2636, KME22D3062, KME22D3275, KME22D3421, KME22D3427, KME22D3712, KME22E2014, KME22F0621, KME22F2238, KME22J3346, KME22K0540, KME22K0541, KME22K0654, KME22K0691, KME22K0694, KME22K0715, KME22K0777, KME22M0921, KME23A0132, KME23A0714, KME23B1443
  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:

Endotracheal Tube oral/nasal Murphy Eye, High Volume, Low Pressure Cuff, REF 112082080

Product Codes/Lot Numbers:

UDI/DI 14026704341440, Batch Numbers: 18GG11, 18GG12, 18GG13, 18GT08, 18GT11, 18HG40, 18IG04, 18IG07, 18IG12, 18IG13, 18IG23, 18IT06, 18IT10, 18IT16, 18JG07, 18JG09, 18JG13, 18JG26, 18JG37, 18JG38, 18JT06, 18JT10, 19AG35, 19AG38, 19AT20, 19BG06, 19BG07, 19BG14, 19BG18, 19BG22, 19BG25, 19BG30, 19BT08, 19BT12, 19DT36, 19DT43, 19ET22, 19ET27, 19ET82, 19ET83, 19FT04, 19FT13, 19FT26, 19FT28, 19KT14, 19LT46, 19LT47, 19LT51, 20AT22, 20AT49, 20BG15, 20BG19, 20BT05, 20BT09, 20BT10, 20BT24, 20CT42, 20CT48, 20CT54, 20DT10, 20DT23, 20DT28, 20ET16, 20ET17, 20ET39, 20FT17, 20FT43, 20FT49, 20FT58, 20FT61, 20GG48, 20GT10, 20GT11, 20GT12, 20GT23, KME20G0436, KME20H0953, KME20L1706, KME20L2207, KME20L2333, KME20L2607, KME20L2696, KME20M1043, KME20M1342, KME21A1435, KME21A1524, KME21A2058, KME21B0616, KME21D1653, KME21D1946, KME21D2011, KME21D2012, KME21E0584, KME21E0687, KME21E1452, KME21F0981, KME21F1006, KME21F1215, KME21F1530, KME21F1604, KME21G0736, KME21G1100, KME21J0109, KME21J0563, KME21J1295, KME21J1364, KME21J1415, KME21J1532, KME21J2055, KME21K0022, KME21K0187, KME21K0449, KME21K2884, KME21K3013, KME21L0744, KME21L1438, KME21L1533, KME21L1661, KME21L1787, KME21L2012, KME21L2177, KME21M3032, KME21M3137, KME21M3236, KME22A0626, KME22A0793, KME22A1043, KME22A1701, KME22A2203, KME22A2429, KME22A2693, KME22A2966, KME22B0500, KME22B0737, KME22B0898, KME22B0915, KME22B0991, KME22C1987, KME22C2072, KME22C2219, KME22C2400, KME22C3376, KME22D0004, KME22D1589, KME22D1689, KME22D1897, KME22D2014, KME22D2505, KME22D2636, KME22D3062, KME22D3275, KME22D3421, KME22D3427, KME22D3712, KME22E2014, KME22F0621, KME22F2238, KME22J3346, KME22K0540, KME22K0541, KME22K0654, KME22K0691, KME22K0694, KME22K0715, KME22K0777, KME22M0921, KME23A0132, KME23A0714, KME23B1443

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: Z-1890-2023

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