Preformed AGT Oral Endotracheal Tube Murphy Eye, High Volume, Low Pressure Cuff, REF 111780065
- Company
- Teleflex Llc
- Recall Initiated
- May 25, 2023
- Posted
- June 29, 2023
- Recall Number
- Z-1946-2023
- Quantity
- 14780 units
- Firm Location
- Morrisville, NC
Reason for Recall
Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.
Distribution
US Nationwide distribution including Puerto Rico.
Lot / Code Info
UDI/DI 14026704341099, Batch Numbers: 18FG12, 18FG23, 18FG24, 18GT26, 18HG24, 18IG11, 18IG14, 18IG24, 18JG07, 18JG36, 18KG10, 18LG11, 18LG31, 19AG11, 19AG36, 19CT36, 19DT10, 19ET12, 19FT18, 19FT49, 19HT03, 19HT66, 19IT43, 19JT20, 19KT21, 19LT08, 19LT31, 20AT49, 20BT53, 20DT14, 20DT24, 20FT59, KME20H0325, KME20J1141, KME20L0727, KME20M0906, KME20M2652, KME21B0072, KME21C0332, KME21C0923, KME21C3299, KME21D0466, KME21D1903, KME21L1006, KME21L1007, KME21M1776, KME21M3025, KME21M3026, KME22A0377, KME22B1011, KME22C1836, KME22C2817, KME22D1076, KME22D2087, KME22F1763, KME22G1315, KME22G3080, KME22H0004, KME22H2233, KME22J1231, KME22J2727, KME22K0999, KME22K1158, KME22K1240, KME22M3068
Root Cause
Under Investigation by firm
Action Taken
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