TELEFLEX LLC Slick Set Cuffed Endotracheal Tube and Stylet Set, oral/nasal, REF 170050 Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Slick Set Cuffed Endotracheal Tube and Stylet Set, oral/nasal, REF 170050
Brand
TELEFLEX LLC
Lot Codes / Batch Numbers
UDI/DI: 4026704319534, Batch numbers: 18FG05, 18GG08, 18GT32, 18HG38, 18JG02, 18JG11, 18KG15, 18LG22, 19AG24, 19DT06, 19DT33, 19ET28, 19FT18, 19IT25, 19KT48, 20AT14, 20DT09, 20ET04, 20GT31, KME20J1235, KME20J1238, KME20K2551, KME20L1089, KME20L2371, KME21A2064, KME21B2498, KME21F1552, KME21G1708, KME21K1248, KME21M2648, KME22B1391, KME22D1768, KME22D1769
Products Sold
UDI/DI: 4026704319534, Batch numbers: 18FG05, 18GG08, 18GT32, 18HG38, 18JG02, 18JG11, 18KG15, 18LG22, 19AG24, 19DT06, 19DT33, 19ET28, 19FT18, 19IT25, 19KT48, 20AT14, 20DT09, 20ET04, 20GT31, KME20J1235, KME20J1238, KME20K2551, KME20L1089, KME20L2371, KME21A2064, KME21B2498, KME21F1552, KME21G1708, KME21K1248, KME21M2648, KME22B1391, KME22D1768, KME22D1769
TELEFLEX LLC is recalling Slick Set Cuffed Endotracheal Tube and Stylet Set, oral/nasal, REF 170050 due to Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.
Recommended Action
Per FDA guidance
Teleflex issued an URGENT MEDICAL DEVICE RECALL notice to its consignees on 05/25/2012 by FedEx. The notice explained the problem, the risk, and requested the following: Users should cease use and distribution of affected product and immediately quarantine the affected product. Distributors were directed to cease use, distribution, and quarantine the product, and to notify their customers. Teleflex is seeking the return of the affected product. For further information: Contact: Customer Service, Telephone: 1-866-396-2111 FAX: 1-855-419-8507, Email: Recalls@teleflex.com
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticePage updated: Jan 10, 2026