Product Wiki · Recalls · U.S. FDA — Device Enforcement

Preformed AGT Oral Endotracheal Tube Murphy Eye, High Volume, Low Pressure Cuff, REF 111780040 — recall Z-1941-2023

U.S. FDA — Device Enforcement · United States · 2023-05-25 · Class I

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-1941-2023
Date of alert
2023-05-25
Country / jurisdiction
United States
Risk level
Class I
Risk type
recall
Brand
TELEFLEX LLC
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
14026704341044
Reported risk: Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.
Primary source: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?start_search=1&

Verify each fact at the issuing agency before acting. Recall scope, affected lots, and remediation instructions may be updated by the agency after our last sync.

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