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Acclarent, Inc. recalls RELIEVA FLEX Sinus Guide Catheter F-70. Catalog number GC070RF. Product Usage - Sinus Catheter - Intended to provide
Recalled June 17, 2015 · FDA recall Z-1740-2015 · Acclarent
Hazard
Acclarent determined that one single RELIEVA FLEX Sinus Guide Catheter was distributed past it's expiry date. · FDA Class III
Units
986
Sold at
US in the state of Texas
Description
Acclarent determined that one single RELIEVA FLEX Sinus Guide Catheter was distributed past it's expiry date.
Product
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. .
Manufacturer(s)
Acclarent, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →