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 Incorrect labeling; the box label indicates Pediatric, the...
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, Pediatric Nasal Cannula, Non-Flared Prongs, Rx only,
Quantity: 1150 units
Why Was This Recalled?
Incorrect labeling; the box label indicates Pediatric, the product insert indicates an Adult device.
Where Was This Sold?
This product was distributed to 20 states: CA, CT, FL, IL, IN, MD, MI, MN, MS, MO, NV, NJ, NY, NC, OH, PA, TX, VA, WV, WI
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