TELEFLEX LLC recalls Endotracheal Tube oral/nasal Murphy Eye, High Volume, Low Pr
Recalled Product
Endotracheal Tube oral/nasal Murphy Eye, High Volume, Low Pressure Cuff, REF 112082050
Hazard / Issue
Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.
Issued by
FDA
Distribution: Nationwide (United States)
Lot/Code Info: UDI/DI 14026704341389, Batch Numbers: 18GG02, 18GG19, 18GG23, 18GT06, 18JG04, 18JG15, 18JG16, 18JG18, 18JT06, 18JT16, 19AG33, 19AT20, 19BG02, 19BG03, 19BG10, 19BG15, 19BG22, 19BG26, 19BG42, 19BT04, 19CT25, 19CT82, 19DT05, 19FT38, 19IT26, 19JT18, 19LT13, 19LT17, 19LT50, 20AT13, 20AT40, 20BT38, 20CT02, 20CT12, 20CT43, 20DT13, 20ET12, 20ET17, 20ET56, 20FT23, 20GG47, 20GT32, KME20J1385, KME21G1704, KME21G1949, KME21K0151, KME21K0292, KME21M2075, KME21M2306, KME21M2649, KME22A1589, KME22A2197, KME22B1848, KME22B2478, KME22B2538, KME22B2578, KME22B2692, KME22C0066, KME22C0571, KME22D0281, KME22D2503, KME22D2504, KME22E0316, KME22E1277, KME22E1422, KME22E2743, KME22E2879, KME22G0063, KME22J0616, KME22J1331, KME22J1463, KME22K0660, KME22L1657, KME23A2133, KME23A2214, KME23A2221, KME23A2299, KME23A2358, KME23C0172
View official government recall
Were you affected by this recall?
If you were harmed by a recalled product, you may have legal options. Consider speaking with a consumer protection lawyer in your state.
Looking for safe alternatives?
Browse certified-safe products in this category on Amazon →
Get the next US recall alert before it hits the news.
Free. Weekly digest or instant alerts. Unsubscribe anytime.
CAN-SPAM compliant · No spam · Unsubscribe anytime