Slick Set Uncuffed Endotracheal Tube and Stylet Set, oral/nasal, REF 170145

Class I - Dangerous

What Should You Do?

  1. Check if you have this product:
    UDI/DI 14026704644923, Batch Numbers: 18JG14, 18LG15, 19AG24, 19BG12, 19BG16, 19CT49, 19IT25, 20BT05, 20CT12, 20CT51, 20DT29, 20GG41, KME20H2929, KME20K1886, KME20K2586, KME20L1488, KME20L2377, KME21A1891, KME21C0019, KME21C1566, KME21C1974, KME21D0445, KME21J1149, KME21M1818, KME21M2952, KME22D1896, KME22E1744
  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 170145

Product Codes/Lot Numbers:

UDI/DI 14026704644923, Batch Numbers: 18JG14, 18LG15, 19AG24, 19BG12, 19BG16, 19CT49, 19IT25, 20BT05, 20CT12, 20CT51, 20DT29, 20GG41, KME20H2929, KME20K1886, KME20K2586, KME20L1488, KME20L2377, KME21A1891, KME21C0019, KME21C1566, KME21C1974, KME21D0445, KME21J1149, KME21M1818, KME21M2952, KME22D1896, KME22E1744

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: Z-1842-2023

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