PlainRecalls

Accriva Diagnostics, Inc.

Compiled from official public sources by the publisher.

6 recalls on record · Latest: Jun 24, 2026

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Agency notice ledger

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

#2,063 of 14,151 · 6 notices · 0.006% archive

  • BOOK 6 notices
  • RANK #2,063 of 14,151
  • SHARE 0.006% archive
  • AGENCY FDA Devices (6)
  • CAT medical devices
  • CATS 1 category
  • LATEST Jun 24, 2026
  • PHOTO 1908 Brands

Nearest notice-volume peer: 1908 Brands (0 notice gap)

Accriva Diagnostics, Inc. accounts for about 0.006% of the 104,423-notice archive on 6 distinct filings — a mid share signal beside absolute volume. FDA · CPSC · USDA FSIS · NHTSA notice stamps for this firm. Read with this firm → · Dominant category → · Similar-volume firm →

Where Accriva Diagnostics, Inc. sits among 14,151 recalling firms

Accriva Diagnostics, Inc. ranks 2,063rd of 14,151 tracked firms by distinct recall-event count. Archive size reflects filing volume, not inherent product danger.

Accriva Diagnostics, Inc. vs all firms by recall-notice count

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

6 2063rd of 14151 higher than 11,804 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

Accriva Diagnostics, Inc. in the notice-volume neighbourhood

Distinct federal recall events among this firm and nearest nationwide peers

notices

What this shows Accriva Diagnostics, Inc. holds about 0.006% of archive notices alongside 6 distinct filings.

Source FDA · CPSC · USDA FSIS · NHTSA filings aggregated by PlainRecalls As of September 2026
FDA Devices Moderate Jun 24, 2026

directCHECK ACT-LR whole blood quality control, level 2 Model/Catalog Number: DCGLR-2
FDA Devices Moderate Dec 10, 2025

Hemochron Activated Clotting Time Low-Range Test Cuvette, REF: ACT-LR, to be used with the Hemochron Signature ELITE Whole Blood Microcoagulation System
FDA Devices Low Nov 19, 2025

VerifyNow PRUTest Platelet Reactivity Test REF 85225 UDI-DI code: 10711234150078 The VerifyNow PRUTest is a whole blood test used in the laboratory or point of care setting to measure the level of platelet P2Y12 receptor blockade.
FDA Devices Moderate Jan 22, 2025

VerifyNow P2Y12 Platelet Reactivity Test, REF: 85064
FDA Devices Moderate Nov 6, 2024

AVOXimeter 1000E, Product Number: AVOX1000E. The AVOXimeter 1000E is a battery-operated bedside whole blood oximeter.
FDA Devices Moderate Jun 1, 2022

The VerifyNow P2Y12 Test is designed to measure platelet P2Y12 receptor blockade. Substances known to specifically block the P2Y12 receptor include ticagrelor and the thienopyridine class of drugs, including clopidogrel and prasugrel.1-8 The test is based upon the ability of activated platelets to bind fibrinogen. Fibrinogen-coated microparticles aggregate in whole blood in proportion to the number of expressed platelet GP IIb/IIIa receptors. Light transmittance increases as activated platelets

Accriva Diagnostics, Inc. holds a measurable archive slice

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

Similar recall count

Nearest multi-notice firms by distinct-event totals (6 here).

1908 Brands 6 Abbott Molecular 6 Advance Medical Designs, Inc. 6 Air Stream Corp. 6 Aire-Master of America Inc 6

Similar medical devices volume

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

Abbott Molecular 6 Advance Medical Designs, Inc. 6 American Medical Systems, Inc. 6 Animas Corporation 6

Frequently Asked Questions

How many federal recall notices name Accriva Diagnostics, Inc.? ▼
PlainRecalls indexes 6 distinct federal recall events naming Accriva Diagnostics, 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 Accriva Diagnostics, Inc. sit among other recalling firms? ▼
Accriva Diagnostics, Inc. ranks #2,063 of 14,151 by distinct recall-event count among 14,151 firms in this archive (83rd percentile of firms with fewer notices). Rank tracks filing frequency, not product danger.
Which agency issues most of Accriva Diagnostics, Inc.'s notices? ▼
FDA Devices accounts for 6 of this firm's 6 indexed notices.
What product category dominates Accriva Diagnostics, Inc.'s filing book? ▼
Filings for Accriva Diagnostics, 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.
Accriva Diagnostics, Inc.: 6 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 Accriva Diagnostics, Inc.; individual notices remain authoritative on each linked recall page.

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