PlainRecalls

Sekisui Diagnostics P.e.i. Inc.

Compiled from official public sources by the publisher.

2 recalls on record · Latest: Feb 1, 2017

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Agency notice ledger

Federal filing book Sekisui Diagnostics P.e.i.… LIGHT-BOOK · SINGLE-AGENCY

#5,725 of 14,151 · 2 notices · 0.002% archive

  • BOOK 2 notices
  • RANK #5,725 of 14,151
  • SHARE 0.002% archive
  • AGENCY FDA Devices (2)
  • CAT medical devices
  • CATS 1 category
  • LATEST Feb 1, 2017
  • PHOTO 3M Company

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

Sekisui Diagnostics P.e.i. 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 →

Sekisui Diagnostics P.e.i.…'s standing among 14,151 recalling firms

Sekisui Diagnostics P.e.i. Inc. ranks 5,725th of 14,151 tracked firms by distinct recall-event count. Archive size reflects filing volume, not inherent product danger.

Sekisui Diagnostics P.e.i.… vs all firms by recall-notice count

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

2 5725th 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 · 2026-09-19

Sekisui Diagnostics P.e.i.… in the notice-volume neighbourhood

Distinct federal recall events among this firm and nearest nationwide peers

notices

What this shows Sekisui Diagnostics P.e.i. 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 Feb 1, 2017

Sekisui Diagnostics Ammonia L3K¿ Assay; Catalog Number: 293-80-91 and 293-10 For the IN VITRO quantitative measurement of ammonia concentration in plasma
FDA Devices Moderate Mar 23, 2016

Sekure Chemistry Sekisui Diagnostics Acetaminophen L3K Assay, In-vitro Diagnostic Catalog Number: 506-10: R1: 1 x 10ml, R2: 2 x 10ml Catalog Number: 506-30: R1: 3 x 10ml, R2: 6 x 10ml In-Vitro quantitative measurement of Acetaminophen in serum and plasma used m the diagnosis and treatment of acetaminophen overdose toxicity.

Sekisui Diagnostics P.e.i.… 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.

3M Company 2 3M Company/3m Espe Dental Products 2 A.o. Smith Electrical Products Co., of Tipp City, Ohio 2 Abbott GmbH 2

Frequently Asked Questions

How many federal recall notices name Sekisui Diagnostics P.e.i.…? ▼
PlainRecalls indexes 2 distinct federal recall events naming Sekisui Diagnostics P.e.i. 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 Sekisui Diagnostics P.e.i.… sit among other recalling firms? ▼
Sekisui Diagnostics P.e.i. Inc. ranks #5,725 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 Sekisui Diagnostics P.e.i.…'s notices? ▼
FDA Devices accounts for 2 of this firm's 2 indexed notices.
What product category dominates Sekisui Diagnostics P.e.i.…'s filing book? ▼
Filings for Sekisui Diagnostics P.e.i. 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.
Sekisui Diagnostics P.e.i. 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 Sekisui Diagnostics P.e.i. Inc.; individual notices remain authoritative on each linked recall page.

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