Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Sengstaken Tube and Sengstaken-Blakemore Tube. Teleflex product codes 204800 Recalled by Teleflex Medical Due to Sterility of the product cannot be guaranteed.
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
Sengstaken Tube and Sengstaken-Blakemore Tube. Teleflex product codes 204800, 204802, and 204803, a gastrointestinal tube and accessories, consisting of flexible or semi-rigid tubing used for instilling fluids into, withdrawing fluids from, splinting, or suppressing bleeding of the alimentary tract.
Quantity: 117,801 ea.
Why Was This Recalled?
Sterility of the product cannot be guaranteed.
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