Serious health hazard — there is a reasonable probability that use of or exposure to this product will cause serious adverse health consequences or death.
Preformed AGT Oral Endotracheal Tube Murphy Eye Recalled by TELEFLEX LLC Due to Reports of disconnection of the 15mm connector from...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact TELEFLEX LLC directly.
Affected Products
Preformed AGT Oral Endotracheal Tube Murphy Eye, High Volume, Low Pressure Cuff, REF 111781080
Quantity: 8620 units
Why Was This Recalled?
Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About TELEFLEX LLC
TELEFLEX LLC has 139 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report