🔍 RecallPedia

Slick Set Uncuffed Endotracheal Tube and Stylet Set, oral/nasal, REF 170140

Class I - Dangerous
🏥 Medical Devices Recalled: May 25, 2023 TELEFLEX Other Medical Devices Nationwide

What Should You Do?

  1. Check if you have this product:
    UDI/DI 14026704647047, Batch Numbers: 18JG17, 18JG32, 18JG34, 18KG29, 18LG02, 18LG15, 18LG18, 19AG09, 19AG21, 19BG12, 19CT32, 19DT06, 19DT20, 19ET38, 19ET72, 19ET77, 19FT24, 19JT29, 20BG16, 20CT36, 20DT37, 20ET28, 20GG45, 20GT14, KME20H2017, KME20K0772, KME20K2549, KME20K2584, KME20L1491, KME20L2402, KME21A1159, KME21A1900, KME21A2810, KME21B0572, KME21B1688, KME21C0024, KME21C0493, KME21C2999, KME21L1921, KME21L1922, KME22B1077, KME22C2262, KME22C3452, KME22E1239, KME22F0049, KME22F1951, KME22H0913, KME22H0967, KME22H2910
  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 170140

Product Codes/Lot Numbers:

UDI/DI 14026704647047, Batch Numbers: 18JG17, 18JG32, 18JG34, 18KG29, 18LG02, 18LG15, 18LG18, 19AG09, 19AG21, 19BG12, 19CT32, 19DT06, 19DT20, 19ET38, 19ET72, 19ET77, 19FT24, 19JT29, 20BG16, 20CT36, 20DT37, 20ET28, 20GG45, 20GT14, KME20H2017, KME20K0772, KME20K2549, KME20K2584, KME20L1491, KME20L2402, KME21A1159, KME21A1900, KME21A2810, KME21B0572, KME21B1688, KME21C0024, KME21C0493, KME21C2999, KME21L1921, KME21L1922, KME22B1077, KME22C2262, KME22C3452, KME22E1239, KME22F0049, KME22F1951, KME22H0913, KME22H0967, KME22H2910

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: Z-1841-2023

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