Skip to content
Recall Observatory FDA recall evidence

Device product

Endotracheal Tube oral/nasal uncuffed/plain - Magill, REF 100380035

Z-1927-2023

May 25, 2023

Class I

Product summary

Firm
TELEFLEX LLC
Event
Event 92373
Status
Ongoing
Classification
Class I
Quantity
2860 units
Official record key
device-enforcement:Z-1927-2023

Official wording

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

Code information: UDI/DI 14026704340634, Batch Numbers: 18HG08, 18IG13, 18JG35, 18LG31, 19BG15, 19CT16, 19ET31, 19HT07, 19HT79, 19LT28, 20GT37, KME20H2590, KME20L0690, KME22D0945, KME22E1145, KME22G2935, KME22J0819, KME22J2900

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.