Slick Set Uncuffed Endotracheal Tube and Stylet Set, oral/nasal, REF 170135
Class I - DangerousWhat Should You Do?
- Check if you have this product: UDI/DI 14026704647030, Batch Numbers: 18KG03, 18KG07, 18KG18, 18LG22, 19AG18, 19AG21, 19AG24, 19AG37, 19BG04, 19BG12, 19BG40, 19CT49, 19CT58, 19DT06, 19DT20, 19DT38, 19ET22, 19ET28, 19GT45, 19GT59, 19GT65, 19HT05, 19HT35, 19HT61, 19HT66, 19IT54, 19JT22, 19JT29, 20AT32, 20AT53, 20BT05, 20BT23, 20BT47, 20CT12, 20CT36, 20DT09, 20DT37, 20ET16, 20ET21, 20ET28, KME20G0242, KME20H1846, KME20J0328, KME20J1234, KME20K1629, KME20K2547, KME20K2583, KME20K3590, KME20L0632, KME20L1486, KME20L2401, KME20M0811, KME20M3276, KME20M3277, KME21A1898, KME21A2813, KME21B1686, KME21C0018, KME21D1850, KME21E0464, KME21K1250, KME21L1893, KME21L1894, KME21L2343, KME22A0207, KME22A1510, KME22B0538, KME22B0726, KME22B1029, KME22B2334, KME22C1825, KME22C2261, KME22E2104, KME22E2263, KME22E2264, KME22F2163, KME22F2418, KME22H0050, KME22H0350, KME22H2625, KME22J0996
- 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 Uncuffed Endotracheal Tube and Stylet Set, oral/nasal, REF 170135
Product Codes/Lot Numbers:
UDI/DI 14026704647030, Batch Numbers: 18KG03, 18KG07, 18KG18, 18LG22, 19AG18, 19AG21, 19AG24, 19AG37, 19BG04, 19BG12, 19BG40, 19CT49, 19CT58, 19DT06, 19DT20, 19DT38, 19ET22, 19ET28, 19GT45, 19GT59, 19GT65, 19HT05, 19HT35, 19HT61, 19HT66, 19IT54, 19JT22, 19JT29, 20AT32, 20AT53, 20BT05, 20BT23, 20BT47, 20CT12, 20CT36, 20DT09, 20DT37, 20ET16, 20ET21, 20ET28, KME20G0242, KME20H1846, KME20J0328, KME20J1234, KME20K1629, KME20K2547, KME20K2583, KME20K3590, KME20L0632, KME20L1486, KME20L2401, KME20M0811, KME20M3276, KME20M3277, KME21A1898, KME21A2813, KME21B1686, KME21C0018, KME21D1850, KME21E0464, KME21K1250, KME21L1893, KME21L1894, KME21L2343, KME22A0207, KME22A1510, KME22B0538, KME22B0726, KME22B1029, KME22B2334, KME22C1825, KME22C2261, KME22E2104, KME22E2263, KME22E2264, KME22F2163, KME22F2418, KME22H0050, KME22H0350, KME22H2625, KME22J0996
Official Source
Always verify recall information with the official FDA source:
View on FDA.govFDA Recall Number: Z-1840-2023
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