Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Propel Mini Mometasone Furoate Sinus Implant Recalled by Intersect ENT, Inc. Due to Sinus Implant product label displays incorrect product information...
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 Intersect ENT, Inc. directly.
Affected Products
Propel Mini Mometasone Furoate Sinus Implant, with Straight Delivery System, REF 60044
Quantity: 611 units
Why Was This Recalled?
Sinus Implant product label displays incorrect product information including: "Straight Delivery System", with incorrect reference number and UDI-DI.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Intersect ENT, Inc.
Intersect ENT, Inc. has 2 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report