Skip to content
Recall Observatory FDA recall evidence

Device product

Slick Set Cuffed Endotracheal Tube and Stylet Set, oral/nasal, REF 170060

Z-1829-2023

May 25, 2023

Class I

Product summary

Firm
TELEFLEX LLC
Event
Event 92373
Status
Ongoing
Classification
Class I
Quantity
9400 units
Official record key
device-enforcement:Z-1829-2023

Official wording

Reason: Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.

Code information: UDI/DI 4026704319558, Batch numbers: 18GG31, 18HG22, 18HG32, 18HG35, 18IG09, 18IG24, 18IG27, 18JG17, 18LG12, 19AG37, 19BG12, 19CT49, 19DT15, 19DT20, 19ET22, 19ET38, 19ET77, 19FT18, 19IT14, 19IT25, 19JT42, 20DT29, 20ET04, 20FT34, 20FT54, 20GG41, KME20H1653, KME20J1236, KME20J1237, KME20L1487, KME20L2379, KME20M0494, KME21A0384, KME21A1482, KME21C0293, KME21E1411, KME21G0757, KME21G2208, KME21G2209, KME21K0548, KME21K0549, KME21L0444, KME21M1392, KME22A1512, KME22A1513, KME22B1392

Distribution pattern: US Nationwide distribution including Puerto Rico.

Derived failure modes

  • Unknown

    reason.no_named_rule · v1.0.0

    Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.