PlainRecalls

Laserex Systems Inc.

Compiled from official public sources by the publisher.

2 recalls on record · Latest: Jun 14, 2017

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Agency notice ledger

Federal filing book Laserex Systems Inc. LIGHT-BOOK · SINGLE-AGENCY

#5,195 of 14,151 · 2 notices · 0.002% archive

  • BOOK 2 notices
  • RANK #5,195 of 14,151
  • SHARE 0.002% archive
  • AGENCY FDA Devices (2)
  • CAT medical devices
  • CATS 1 category
  • LATEST Jun 14, 2017
  • PHOTO 3M Company

Nearest notice-volume peer: 3M Company, of St. Paul, Minn. (0 notice gap)

Laserex Systems 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 →

Laserex Systems Inc.'s standing among 14,151 recalling firms

Laserex Systems Inc. ranks 5,195th of 14,151 tracked firms by distinct recall-event count. Archive size reflects filing volume, not inherent product danger.

Laserex Systems Inc. vs all firms by recall-notice count

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

2 5195th 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 · 2026-09-16

Laserex Systems Inc. in the notice-volume neighbourhood

Distinct federal recall events among this firm and nearest nationwide peers

notices

What this shows Laserex Systems 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 Moderate Jun 14, 2017

Ellex Tango Reflex with slit lamp Laser Ophthalmic In the SLT mode, the device is intended to be used for selective laser trabeculoplasty (ST) operations (laser trabeculoplasty for primary open angle glaucoma). In the VAG mode it is intended to be used to perform procedures requiring the rupture of tissue in the eye for Iridotomy and Iridectomy, Posterior capsulotomy and Posterior membranectomy.
FDA Devices Moderate Apr 13, 2016

Ellex Medical Fixed eye Safety filters Model Integre S LP5532. The filter is located in the binocular mount of the laser delivery head. The filter prevents transmission of treatment laser light to physician eyes while the aiming beam to remain visible. .

Laserex Systems 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 Laserex Systems Inc.? ▼
PlainRecalls indexes 2 distinct federal recall events naming Laserex Systems 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 Laserex Systems Inc. sit among other recalling firms? ▼
Laserex Systems Inc. ranks #5,195 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 Laserex Systems Inc.'s notices? ▼
FDA Devices accounts for 2 of this firm's 2 indexed notices.
What product category dominates Laserex Systems Inc.'s filing book? ▼
Filings for Laserex Systems 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.
Laserex Systems 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 Laserex Systems Inc.; individual notices remain authoritative on each linked recall page.

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