PlainRecalls

Tekia, Inc.

Compiled from official public sources by the publisher.

2 recalls on record · Latest: Dec 25, 2019

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Agency notice ledger

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

#5,897 of 14,151 · 2 notices · 0.002% archive

  • BOOK 2 notices
  • RANK #5,897 of 14,151
  • SHARE 0.002% archive
  • AGENCY FDA Devices (2)
  • CAT medical devices
  • CATS 1 category
  • LATEST Dec 25, 2019
  • PHOTO 3M Company

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

Tekia, 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 →

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

Tekia, Inc. ranks 5,897th of 14,151 tracked firms by distinct recall-event count. Archive size reflects filing volume, not inherent product danger.

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

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

2 5897th 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

Tekia, Inc. in the notice-volume neighbourhood

Distinct federal recall events among this firm and nearest nationwide peers

notices

What this shows Tekia, 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 Dec 25, 2019

TEKIA Model 872 Single Piece Hydrophilic Acrylic Intraocular Lenses, Diopter 15.0, Sterile. The firm name on the label is TEKIA, INC., Irvine, CA.
FDA Devices Moderate Nov 18, 2015

TEKIA Single Piece Hydrophilic Acrylic Intraocular Lenses, Model 811

Tekia, 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 Tekia, Inc.? ▼
PlainRecalls indexes 2 distinct federal recall events naming Tekia, 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 Tekia, Inc. sit among other recalling firms? ▼
Tekia, Inc. ranks #5,897 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 Tekia, Inc.'s notices? ▼
FDA Devices accounts for 2 of this firm's 2 indexed notices.
What product category dominates Tekia, Inc.'s filing book? ▼
Filings for Tekia, 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.
Tekia, 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 Tekia, Inc.; individual notices remain authoritative on each linked recall page.

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