PlainRecalls

Instratek, Incorporated

Compiled from official public sources by the publisher.

3 recalls on record · Latest: Dec 30, 2015

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Agency notice ledger

Federal filing book Instratek, Incorporated LIGHT-BOOK · SINGLE-AGENCY

#3,697 of 14,151 · 3 notices · 0.003% archive

  • BOOK 3 notices
  • RANK #3,697 of 14,151
  • SHARE 0.003% archive
  • AGENCY FDA Devices (3)
  • CAT medical devices
  • CATS 1 category
  • LATEST Dec 30, 2015
  • PHOTO 3B Medical, Inc.

Nearest notice-volume peer: 3B Medical, Inc. (0 notice gap)

Instratek, Incorporated accounts for about 0.003% of the 104,423-notice archive on 3 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 →

Instratek, Incorporated's standing among 14,151 recalling firms

Instratek, Incorporated ranks 3,697th of 14,151 tracked firms by distinct recall-event count. Archive size reflects filing volume, not inherent product danger.

Instratek, Incorporated vs all firms by recall-notice count

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

3 3697th of 14151 higher than 9,908 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

Instratek, Incorporated in the notice-volume neighbourhood

Distinct federal recall events among this firm and nearest nationwide peers

notices

What this shows Instratek, Incorporated holds about 0.003% of archive notices alongside 3 distinct filings.

Source FDA · CPSC · USDA FSIS · NHTSA filings aggregated by PlainRecalls As of September 2026
FDA Devices Moderate Dec 30, 2015

Hook Blade, Angled. Part number 7058A. Sterile disposable blade for use with Endoscopic Tarsal Tunnel Decompression (ETTD) System.
FDA Devices Moderate Oct 1, 2014

Mini Cannulated Titanium Headed and Headless Screw Set and 2.5, 3.0, and 4.0 mm countersink/depth gauges in the Mini Screw Set/System
FDA Devices Moderate Mar 20, 2013

Endotrig Trigger Release Sterile Micro Hook Blade Product Usage: The blade is intended to release A-1 pulley in endoscopic trigger release procedures.

Instratek, Incorporated is a small archive contributor

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

Similar medical devices volume

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

3B Medical, Inc. 3 A L I Technologies Ltd 3 Abeon Medical Corporation 3 Acist Medical Systems 3

Frequently Asked Questions

How many federal recall notices name Instratek, Incorporated? ▼
PlainRecalls indexes 3 distinct federal recall events naming Instratek, Incorporated, 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 Instratek, Incorporated sit among other recalling firms? ▼
Instratek, Incorporated ranks #3,697 of 14,151 by distinct recall-event count among 14,151 firms in this archive (70th percentile of firms with fewer notices). Rank tracks filing frequency, not product danger.
Which agency issues most of Instratek, Incorporated's notices? ▼
FDA Devices accounts for 3 of this firm's 3 indexed notices.
What product category dominates Instratek, Incorporated's filing book? ▼
Filings for Instratek, Incorporated 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.
Instratek, Incorporated: 3 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 Instratek, Incorporated; individual notices remain authoritative on each linked recall page.

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