Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Hudson RCI Recalled by Teleflex Medical Due to Labeling; The affected product packaging is incorrectly labeled...
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
Hudson RCI, Sheridan, Preformed Tracheal Tubes, Cuffed and Uncuffed, Rx Only, Sterile, Teleflex Medical.
Quantity: 300 units
Why Was This Recalled?
Labeling; The affected product packaging is incorrectly labeled as being a cuffed oral ET tube; The correct product labeling is uncuffed nasal ET tube.
Where Was This Sold?
This product was distributed to 12 states: FL, GA, IL, KY, MA, MI, MS, MO, OH, TX, WA, WV
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