Acclarent, Inc. recalls

6 recalls on record · latest: September 21, 2023

Official U.S. recall history for Acclarent, Inc., compiled from official government records.

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Acclarent, Inc. recalls TruDi Navigation System, Model: FG-2000-00, Catalog: ENS022B, when used with TruDi Curette, Models: TDC0005Z and TDC0005

September 21, 2023 · Medical device recalls Moderate risk When using affected curette and software, there is a discrepancy between the ac…

Acclarent, Inc. recalls TruDi NAV Suction Instruments: 0-Degree, REF: TDNS000Z; 70-Degree, REF: TDNS070Z; and 90-Degree, REF: TDNS090Z

November 12, 2021 · Medical device recalls Moderate risk Suction Instruments were incorrectly calibrated so they may not meet the system…

Acclarent, Inc. recalls TruDi NAV Suction, TDNS070Z, 70 Degree Tip Angle (01) 10705031245884

March 6, 2019 · Medical device recalls Moderate risk The firm became aware that three (3) lots of the NAV Suction Instruments contai…

Acclarent, Inc. recalls TruDi NAV Suction, TDNS090Z, 90 Degree Tip Angle, (01) 10705031245891

March 6, 2019 · Medical device recalls Moderate risk The firm became aware that three (3) lots of the NAV Suction Instruments contai…

Acclarent, Inc. recalls TruDi NAV Suction, TDNS000Z, 0 Degree Tip Angle, (01)10705031245877

March 6, 2019 · Medical device recalls Moderate risk The firm became aware that three (3) lots of the NAV Suction Instruments contai…

Acclarent, Inc. recalls RELIEVA FLEX Sinus Guide Catheter F-70. Catalog number GC070RF. Product Usage - Sinus Catheter - Intended to provide a…

April 28, 2015 · Medical device recalls Acclarent determined that one single RELIEVA FLEX Sinus Guide Catheter was dist…