Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
RUSCH Endotracheal Tube oral/nasal Magill Recalled by Teleflex Medical Europe Ltd Due to The firm received reports that the endotracheal tube...
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 Medical Europe Ltd directly.
Affected Products
RUSCH Endotracheal Tube oral/nasal Magill, High Volume, Low Pressure Cuff, REF numbers: a) 112080050 b) 112080055 c) 112080060 d) 112080065 e) 112080070 f) 112080075 g) 112080080 h) 112080085 i) 112080090 j) 112080095 k) 112080100
Quantity: 2610 units
Why Was This Recalled?
The firm received reports that the endotracheal tube cuff could be inflated while the pilot balloon remained flat.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Teleflex Medical Europe Ltd
Teleflex Medical Europe Ltd has 11 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report