Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
R¿SCH Curved Reinforced Endotracheal Tube: Rusch Reinforced Endotracheal Tube is Recalled by Teleflex, Inc. Due to Teleflex Medical has issued an advisory notification for...
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, Inc. directly.
Affected Products
R¿SCH Curved Reinforced Endotracheal Tube: Rusch Reinforced Endotracheal Tube is designated for oral or nasal intubation and are indicated for airway management. The product may be used to reduce the potential for kinking whenever an unusual positioning of the head or neck is required following intubation.
Quantity: 2,292,361
Why Was This Recalled?
Teleflex Medical has issued an advisory notification for the RUSCH Curved Reinforced Endotracheal Tube because of a discrepancy between the labeled cuff diameter and the actual cuff diameter. The actual product cuff diameter meets required specification.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Teleflex, Inc.
Teleflex, Inc. 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