Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Teleflex Green Non-Latex Robertazzi Nasopharyngeal Airway Recalled by Teleflex Medical Due to Labeling error
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
Teleflex Green Non-Latex Robertazzi Nasopharyngeal Airway, Catalog No. 123130 and 123132 Product Usage: To provide a patent airway for a patient with a blockage or potential blockage of the nasal cavity or nasopharynx.
Quantity: 7,600 eaches
Why Was This Recalled?
Labeling error
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