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Recall Observatory FDA recall evidence

Device product

Preformed AGT Oral Endotracheal Tube uncuffed/plain - Murphy, REF 100181065

Z-1924-2023

May 25, 2023

Class I

Product summary

Firm
TELEFLEX LLC
Event
Event 92373
Status
Ongoing
Classification
Class I
Quantity
2980 units
Official record key
device-enforcement:Z-1924-2023

Official wording

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

Code information: UDI/DI 14026704340597, Batch Numbers: 18FT35, 18GG25, 18JG35, 18KG21, 18LG18, 19AG25, 19CT33, 19ET69, 20BT02, 20CT11, KME22B1670, KME22E1010, KME22E1408, KME22H0137, KME22J0202, KME22K2262

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.