Slick Set Cuffed Endotracheal Tube and Stylet Set, oral/nasal, REF 170080
Class I - DangerousWhat Should You Do?
- 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
- 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 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.govFDA Recall Number: Z-1833-2023
Related Recalls
There are incomplete pre-cleaning instructions within the Instructions for Use (IFU).
There are incomplete pre-cleaning instructions within the Instructions for Use (IFU).
There are incomplete pre-cleaning instructions within the Instructions for Use (IFU).