Low risk — use of or exposure to this product is not likely to cause adverse health consequences.
RELIEVA FLEX Sinus Guide Catheter F-70. Catalog number GC070RF. Product Recalled by Acclarent, Inc. Due to Acclarent determined that one single RELIEVA FLEX Sinus...
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 Acclarent, Inc. directly.
Affected Products
RELIEVA FLEX Sinus Guide Catheter F-70. Catalog number GC070RF. Product Usage - Sinus Catheter - Intended to provide a means to access the sinus space for diagnostic and therapeutic procedures. .
Quantity: 986
Why Was This Recalled?
Acclarent determined that one single RELIEVA FLEX Sinus Guide Catheter was distributed past it's expiry date.
Where Was This Sold?
US in the state of Texas
About Acclarent, Inc.
Acclarent, Inc. has 13 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report