PlainRecalls

Endologix, Inc.

Compiled from official public sources by the publisher.

2 recalls on record · Latest: Jun 17, 2020

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Agency notice ledger

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

#4,764 of 14,151 · 2 notices · 0.002% archive

  • BOOK 2 notices
  • RANK #4,764 of 14,151
  • SHARE 0.002% archive
  • AGENCY FDA Devices (2)
  • CAT medical devices
  • CATS 1 category
  • LATEST Jun 17, 2020
  • PHOTO 3M Company

Nearest notice-volume peer: 3M Company (0 notice gap)

Endologix, Inc. accounts for about 0.002% of the 104,423-notice archive on 2 distinct filings — a light share signal beside absolute volume. FDA · CPSC · USDA FSIS · NHTSA notice stamps for this firm. Read with this firm → · Dominant category → · Similar-volume firm →

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

Endologix, Inc. ranks 4,764th of 14,151 tracked firms by distinct recall-event count. Archive size reflects filing volume, not inherent product danger.

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

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

2 4764th of 14151 higher than 8,037 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

Endologix, Inc. in the notice-volume neighbourhood

Distinct federal recall events among this firm and nearest nationwide peers

notices

What this shows Endologix, Inc. holds about 0.002% of archive notices alongside 2 distinct filings.

Source FDA · CPSC · USDA FSIS · NHTSA filings aggregated by PlainRecalls As of September 2026
FDA Devices Critical Jun 17, 2020

Ovation iX Abdominal Stent Graft Systems, REF: TV-AB2080-I, TV-AB2080-J, TV-AB2380-I, TV-AB2380-J, TV-AB2680-I, TV-AB2680-J, TV-AB2980-I, TV-AB2980-J, TV-AB3480-I, TV-AB3480-J
FDA Devices Critical Jun 19, 2013

Brand Name: AFX" Introducer System, Model Number S17-45. Lot Numbers: 1079840, 1079843, 1079844, 1079845. Product Usage: The AFX Introducer System is intended for use to facilitate the introduction of catheters and other medical devices into the vasculature and to minimize blood loss associated with such introduction.

Endologix, Inc. is a small archive contributor

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

Frequently Asked Questions

How many federal recall notices name Endologix, Inc.? ▼
PlainRecalls indexes 2 distinct federal recall events naming Endologix, 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 Endologix, Inc. sit among other recalling firms? ▼
Endologix, Inc. ranks #4,764 of 14,151 by distinct recall-event count among 14,151 firms in this archive (57th percentile of firms with fewer notices). Rank tracks filing frequency, not product danger.
Which agency issues most of Endologix, Inc.'s notices? ▼
FDA Devices accounts for 2 of this firm's 2 indexed notices.
What product category dominates Endologix, Inc.'s filing book? ▼
Filings for Endologix, 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.
Endologix, Inc.: 2 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 Endologix, Inc.; individual notices remain authoritative on each linked recall page.

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