Slick Set Cuffed Endotracheal Tube and Stylet Set, oral/nasal, REF 170080

Class I - Dangerous

What Should You Do?

  1. Check if you have this product:
    UDI/DI 4026704319596, Batch Numbers: 18FG09, 18FG20, 18FT32, 18GG05, 18GG08, 18GG14, 18HG07, 18HG12, 18HG22, 18HG27, 18HG35, 18IG02, 18IG09, 18IG15, 18JG04, 18JG06, 18JG14, 18JG26, 18LG12, 18LG18, 19AG13, 19AG24, 19AG27, 19AG31, 19BG01, 19CT41, 19DT38, 19ET38, 19ET45, 19ET50, 19FT24, 19GT59, 19IT06, 19IT25, 19IT54, 19JT42, 19JT49, 19JT57, 19KT25, 19LT04, 20AT14, 20AT25, 20AT32, 20AT37, 20AT53, 20BT05, 20BT47, 20CT05, 20CT12, 20CT27, 20CT36, 20CT51, 20DT09, 20FT44, 20GT25, KME20H0248, KME20H2019, KME20L0396, KME20L1278, KME20L1279, KME20L2830, KME20M0847, KME21A0386, KME21A2800, KME21A2801, KME21B1245, KME21B2156, KME21C0533, KME21D1204, KME21E1287, KME21F1329, KME21J0410, KME21L0274, KME21L0813, KME21L0851, KME22E2351
  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 Cuffed Endotracheal Tube and Stylet Set, oral/nasal, REF 170080

Product Codes/Lot Numbers:

UDI/DI 4026704319596, Batch Numbers: 18FG09, 18FG20, 18FT32, 18GG05, 18GG08, 18GG14, 18HG07, 18HG12, 18HG22, 18HG27, 18HG35, 18IG02, 18IG09, 18IG15, 18JG04, 18JG06, 18JG14, 18JG26, 18LG12, 18LG18, 19AG13, 19AG24, 19AG27, 19AG31, 19BG01, 19CT41, 19DT38, 19ET38, 19ET45, 19ET50, 19FT24, 19GT59, 19IT06, 19IT25, 19IT54, 19JT42, 19JT49, 19JT57, 19KT25, 19LT04, 20AT14, 20AT25, 20AT32, 20AT37, 20AT53, 20BT05, 20BT47, 20CT05, 20CT12, 20CT27, 20CT36, 20CT51, 20DT09, 20FT44, 20GT25, KME20H0248, KME20H2019, KME20L0396, KME20L1278, KME20L1279, KME20L2830, KME20M0847, KME21A0386, KME21A2800, KME21A2801, KME21B1245, KME21B2156, KME21C0533, KME21D1204, KME21E1287, KME21F1329, KME21J0410, KME21L0274, KME21L0813, KME21L0851, KME22E2351

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: Z-1833-2023

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