Slick Set Cuffed Endotracheal Tube and Stylet Set, oral/nasal, REF 170070
Class I - DangerousWhat Should You Do?
- Check if you have this product: UDI/DI 4026704319572, Batch numbers: 18FG09, 18FG15, 18FG17, 18FG20, 18FG21, 18GG10, 18GG28, 18GT32, 18HG07, 18HG16, 18HG35, 18HG38, 18IG09, 18JG02, 18JG17, 18JG37, 18KG23, 18KG35, 18LG05, 18LG12, 18LG18, 19AG13, 19AG31, 19AG34, 19BG04, 19CT17, 19CT41, 19CT49, 19CT55, 19FT24, 19FT41, 19GT05, 19GT10, 19GT52, 19GT59, 19GT65, 19HT40, 19HT66, 19IT44, 19IT54, 19JT22, 19JT42, 19JT57, 19JT64, 19KT30, 19KT41, 19LT04, 19LT17, 20AT14, 20AT25, 20AT44, 20AT53, 20BT05, 20BT23, 20BT47, 20CT05, 20CT12, 20CT27, 20CT51, 20DT09, 20DT37, 20ET16, 20ET56, 20FT10, 20FT54, 20GG36, 20GG45, KME20H0245, KME20H1287, KME20H1288, KME20J0571, KME20J0572, KME20J0802, KME20J3033, KME20K2544, KME20L0053, KME20L0055, KME20L0942, KME20L2372, KME20M0381, KME20M1103, KME20M1755, KME21A0893, KME21B1074, KME21B1075, KME21D1430, KME21E1290, KME21F1526, KME21G0541, KME21G0542, KME21G0543, KME21G1559, KME21H0608, KME21K0551, KME21K1767, KME21K2469, KME21L1897
- Do not eat it: Even if it looks and smells fine, do not consume this product.
- Throw it away or return it: You can return the product to the store for a full refund.
- Seek medical attention if needed: If you've consumed this product and feel unwell, contact your doctor immediately.
- 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 170070
Product Codes/Lot Numbers:
UDI/DI 4026704319572, Batch numbers: 18FG09, 18FG15, 18FG17, 18FG20, 18FG21, 18GG10, 18GG28, 18GT32, 18HG07, 18HG16, 18HG35, 18HG38, 18IG09, 18JG02, 18JG17, 18JG37, 18KG23, 18KG35, 18LG05, 18LG12, 18LG18, 19AG13, 19AG31, 19AG34, 19BG04, 19CT17, 19CT41, 19CT49, 19CT55, 19FT24, 19FT41, 19GT05, 19GT10, 19GT52, 19GT59, 19GT65, 19HT40, 19HT66, 19IT44, 19IT54, 19JT22, 19JT42, 19JT57, 19JT64, 19KT30, 19KT41, 19LT04, 19LT17, 20AT14, 20AT25, 20AT44, 20AT53, 20BT05, 20BT23, 20BT47, 20CT05, 20CT12, 20CT27, 20CT51, 20DT09, 20DT37, 20ET16, 20ET56, 20FT10, 20FT54, 20GG36, 20GG45, KME20H0245, KME20H1287, KME20H1288, KME20J0571, KME20J0572, KME20J0802, KME20J3033, KME20K2544, KME20L0053, KME20L0055, KME20L0942, KME20L2372, KME20M0381, KME20M1103, KME20M1755, KME21A0893, KME21B1074, KME21B1075, KME21D1430, KME21E1290, KME21F1526, KME21G0541, KME21G0542, KME21G0543, KME21G1559, KME21H0608, KME21K0551, KME21K1767, KME21K2469, KME21L1897
Official Source
Always verify recall information with the official FDA source:
View on FDA.govFDA Recall Number: Z-1831-2023
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