Slick Set Uncuffed Endotracheal Tube and Stylet Set, oral/nasal, REF 170135

Class I - Dangerous

What Should You Do?

  1. Check if you have this product:
    UDI/DI 14026704647030, Batch Numbers: 18KG03, 18KG07, 18KG18, 18LG22, 19AG18, 19AG21, 19AG24, 19AG37, 19BG04, 19BG12, 19BG40, 19CT49, 19CT58, 19DT06, 19DT20, 19DT38, 19ET22, 19ET28, 19GT45, 19GT59, 19GT65, 19HT05, 19HT35, 19HT61, 19HT66, 19IT54, 19JT22, 19JT29, 20AT32, 20AT53, 20BT05, 20BT23, 20BT47, 20CT12, 20CT36, 20DT09, 20DT37, 20ET16, 20ET21, 20ET28, KME20G0242, KME20H1846, KME20J0328, KME20J1234, KME20K1629, KME20K2547, KME20K2583, KME20K3590, KME20L0632, KME20L1486, KME20L2401, KME20M0811, KME20M3276, KME20M3277, KME21A1898, KME21A2813, KME21B1686, KME21C0018, KME21D1850, KME21E0464, KME21K1250, KME21L1893, KME21L1894, KME21L2343, KME22A0207, KME22A1510, KME22B0538, KME22B0726, KME22B1029, KME22B2334, KME22C1825, KME22C2261, KME22E2104, KME22E2263, KME22E2264, KME22F2163, KME22F2418, KME22H0050, KME22H0350, KME22H2625, KME22J0996
  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:

Slick Set Uncuffed Endotracheal Tube and Stylet Set, oral/nasal, REF 170135

Product Codes/Lot Numbers:

UDI/DI 14026704647030, Batch Numbers: 18KG03, 18KG07, 18KG18, 18LG22, 19AG18, 19AG21, 19AG24, 19AG37, 19BG04, 19BG12, 19BG40, 19CT49, 19CT58, 19DT06, 19DT20, 19DT38, 19ET22, 19ET28, 19GT45, 19GT59, 19GT65, 19HT05, 19HT35, 19HT61, 19HT66, 19IT54, 19JT22, 19JT29, 20AT32, 20AT53, 20BT05, 20BT23, 20BT47, 20CT12, 20CT36, 20DT09, 20DT37, 20ET16, 20ET21, 20ET28, KME20G0242, KME20H1846, KME20J0328, KME20J1234, KME20K1629, KME20K2547, KME20K2583, KME20K3590, KME20L0632, KME20L1486, KME20L2401, KME20M0811, KME20M3276, KME20M3277, KME21A1898, KME21A2813, KME21B1686, KME21C0018, KME21D1850, KME21E0464, KME21K1250, KME21L1893, KME21L1894, KME21L2343, KME22A0207, KME22A1510, KME22B0538, KME22B0726, KME22B1029, KME22B2334, KME22C1825, KME22C2261, KME22E2104, KME22E2263, KME22E2264, KME22F2163, KME22F2418, KME22H0050, KME22H0350, KME22H2625, KME22J0996

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: Z-1840-2023

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