Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Rusch Brochopart and Rusch Brochopart White The Rush Endobronchial Tube Recalled by Teleflex Medical Due to The product may fail to achieve seal of...
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 directly.
Affected Products
Rusch Brochopart and Rusch Brochopart White The Rush Endobronchial Tube set is indicated for uses commonly associated with oral endobronchial tubes, including, but not limited to, thoracic surgery, bronchospirometry, administration of endobronchial anesthesia, etc. The endobronchial tube allows ventilation and selective inflation or deflation of either lung.
Quantity: 63,568 ea.
Why Was This Recalled?
The product may fail to achieve seal of right lung due to the cuff inflating to one side
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Teleflex Medical
Teleflex Medical has 204 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report