PlainRecalls

Acclarent, Inc.

Compiled from official public sources by the publisher.

13 recalls on record · Latest: Nov 1, 2023

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Agency notice ledger

Federal filing book Acclarent, Inc. LIGHT-BOOK · SINGLE-AGENCY

#1,145 of 14,151 · 13 notices · 0.012% archive

  • BOOK 13 notices
  • RANK #1,145 of 14,151
  • SHARE 0.012% archive
  • AGENCY FDA Devices (13)
  • CAT medical devices
  • CATS 1 category
  • LATEST Nov 1, 2023
  • PHOTO Aequita Pharmacy

Nearest notice-volume peer: Aequita Pharmacy (0 notice gap)

Acclarent, Inc. accounts for about 0.012% of the 104,423-notice archive on 13 distinct filings — a mid share signal beside absolute volume. FDA · CPSC · USDA FSIS · NHTSA notice stamps for this firm. Read with this firm → · Dominant category → · Similar-volume firm →

Acclarent, Inc.'s standing among 14,151 recalling firms

Acclarent, Inc. ranks 1,145th of 14,151 tracked firms by distinct recall-event count. Archive size reflects filing volume, not inherent product danger.

Acclarent, Inc. vs all firms by recall-notice count

Where this firm's archive sits among every tracked recalling manufacturer

13 1145th of 14151 higher than 12,927 of 14,151 firms

Firms, banded by distinct federal recall-event inventory

Each bar is a band; taller bars hold more firms. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source FDA · CPSC · USDA FSIS · NHTSA federal recall filings · 2026-09-13

Acclarent, Inc. in the notice-volume neighbourhood

Distinct federal recall events among this firm and nearest nationwide peers

notices

What this shows Acclarent, Inc. holds about 0.012% of archive notices alongside 13 distinct filings.

Source FDA · CPSC · USDA FSIS · NHTSA filings aggregated by PlainRecalls As of September 2026
FDA Devices Moderate Nov 1, 2023

TruDi Navigation System, Model: FG-2000-00, Catalog: ENS022B, when used with TruDi Curette, Models: TDC0005Z and TDC0005
FDA Devices Moderate Dec 29, 2021

TruDi NAV Suction Instruments: 0-Degree, REF: TDNS000Z; 70-Degree, REF: TDNS070Z; and 90-Degree, REF: TDNS090Z
FDA Devices Moderate Jan 29, 2020

TruDi NAV Suction, TDNS070Z, 70 Degree Tip Angle (01) 10705031245884
FDA Devices Moderate Jan 29, 2020

TruDi NAV Suction, TDNS090Z, 90 Degree Tip Angle, (01) 10705031245891
FDA Devices Moderate Jan 29, 2020

TruDi NAV Suction, TDNS000Z, 0 Degree Tip Angle, (01)10705031245877
FDA Devices Low Jun 17, 2015

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. .
FDA Devices Moderate Aug 7, 2013

Inspira AIR Balloon Dilation system. Size 5 x 24 mm, Syringe volume 6-8 cc. Dilation of airway tree.
FDA Devices Moderate Aug 7, 2013

Inspira AIR Balloon Dilation system. Size 10 x 40 mm, Syringe volume 12 cc. Dilation of airway tree.
FDA Devices Moderate Aug 7, 2013

Inspira AIR Balloon Dilation system. Size 8.5 x 24 mm, Syringe volume 12 cc. Dilation of airway tree.
FDA Devices Moderate Aug 7, 2013

Inspira AIR Balloon Dilation system. Size 12 x 40 mm, Syringe volume 12 cc. Dilation of airway tree.
FDA Devices Moderate Aug 7, 2013

Inspira AIR Balloon Dilation system. Size 14 x 40 mm, Syringe volume 12 cc. Dilation of airway tree.
FDA Devices Moderate Aug 7, 2013

Inspira AIR Balloon Dilation system. Size 16 x 40 mm, Syringe volume 12 cc. Dilation of airway tree.
FDA Devices Moderate Aug 7, 2013

Inspira AIR Balloon Dilation system. Size 7 x 24 mm, Syringe volume 6-8 cc. Dilation of airway tree.

Acclarent, Inc. holds a measurable archive slice

Drug and device firms outside this manufacturer and state, matched by notice volume and category footprint.

Similar recall count

Nearest multi-notice firms by distinct-event totals (13 here — thin-book).

Aequita Pharmacy 13 Alden Optical 13 Amneal Pharmaceuticals, LLC 13 Ani Pharmaceuticals, Inc. 13 AtriCure, Inc. 13

Similar medical devices volume

Nearest multi-notice firms in the same narrow category lane.

Aequita Pharmacy 13 Alden Optical 13 AtriCure, Inc. 13 Augustine Temperature Management, LLC 13

Frequently Asked Questions

How many federal recall notices name Acclarent, Inc.? ▼
PlainRecalls indexes 13 distinct federal recall events naming Acclarent, Inc., aggregated from FDA, CPSC, USDA FSIS, and NHTSA filings (archive as of September 2026). That count is an issuance inventory, not a hazard score.
Where does Acclarent, Inc. sit among other recalling firms? ▼
Acclarent, Inc. ranks #1,145 of 14,151 by distinct recall-event count among 14,151 firms in this archive (91st percentile of firms with fewer notices). Rank tracks filing frequency, not product danger.
Which agency issues most of Acclarent, Inc.'s notices? ▼
FDA Devices accounts for 13 of this firm's 13 indexed notices.
What product category dominates Acclarent, Inc.'s filing book? ▼
Filings for Acclarent, Inc. span 1 product category, led by medical devices. Browse that category archive for peer firms and related notices.
Is a higher notice count more dangerous? ▼
No. Archive size reflects how often federal agencies publish recalls naming the firm — reporting volume, coverage, and product range all move the number. Always verify the individual notice with the issuing agency before acting on a specific product.
Acclarent, Inc.: 13 federal recall notices aggregated from FDA, CPSC, USDA FSIS, and NHTSA filings (lead agency FDA Devices). Verify individual notices with FDA directly before acting on a specific recall.

Firm-level totals aggregate distinct federal recall events naming Acclarent, Inc.; individual notices remain authoritative on each linked recall page.

Methodology · Corrections · FDA · CPSC · USDA FSIS · NHTSA · Archive as of September 2026