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Recall Observatory FDA recall evidence

Device product

Preformed AGT Oral Endotracheal Tube uncuffed/plain - Murphy, REF 100180060

Z-1867-2023

May 25, 2023

Class I

Product summary

Firm
TELEFLEX LLC
Event
Event 92373
Status
Ongoing
Classification
Class I
Quantity
2714 units
Official record key
device-enforcement:Z-1867-2023

Official wording

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

Code information: UDI/DI 14026704340498, Batch Numbers: 18KG08, 18LG33, 19AG21, 19BG12, 19ET12, 19FT19, 19HT34, 19IT12, 19IT43, 19LT32, 20AT49, 20DT15, 20GG27, KME20K1813, KME20L2063, KME20M1586, KME21A2393, KME21C3189, KME22D3370, KME22F2673

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.