Class III — Low Risk

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...

Date: April 28, 2015
Company: Acclarent, Inc.
Status: Terminated
Source: FDA (Device)

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.

Related Recalls

Data sourced from the FDA (Device). Last updated March 26, 2026. View original report