TELEFLEX LLC recalls Preformed AGT Oral Endotracheal Tube Murphy Eye, High Volume
Recalled Product
Preformed AGT Oral Endotracheal Tube Murphy Eye, High Volume, Low Pressure Cuff, REF 111780080
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 14026704341129, Batch Numbers: 18FG33, 18GG23, 18GG34, 18HG30, 18IG11, 18IG18, 18JG21, 18JG35, 18KG19, 18KG41, 19AG15, 19BG04, 19BG19, 19GT65, 19HT68, 19IT15, 19LT21, 20AT26, 20CT12, 20CT13, 20CT32, 20DT35, 20FT19, KME20M3089, KME20M3090, KME21A1299, KME21A2090, KME21B0716, KME21B1783, KME21B1962, KME21B2204, KME21B2676, KME21C0599, KME22B0591, KME22C2317, KME22D0156, KME22D2122, KME22D2752, KME22E1153, KME22G0816, KME22H2094, KME22H2235, KME22H3271, KME22J0148, KME22J0532, KME22J3210, KME22K2844
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