PlainRecalls

Hycor Biomedical Inc

Compiled from official public sources by the publisher.

2 recalls on record · Latest: Aug 14, 2019

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Agency notice ledger

Federal filing book Hycor Biomedical Inc LIGHT-BOOK · SINGLE-AGENCY

#5,031 of 14,151 · 2 notices · 0.002% archive

  • BOOK 2 notices
  • RANK #5,031 of 14,151
  • SHARE 0.002% archive
  • AGENCY FDA Devices (2)
  • CAT medical devices
  • CATS 1 category
  • LATEST Aug 14, 2019
  • PHOTO 3M Company

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

Hycor Biomedical 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 →

How Hycor Biomedical Inc compares to 14,151 recalling firms

Hycor Biomedical Inc ranks 5,031st of 14,151 tracked firms by distinct recall-event count. Archive size reflects filing volume, not inherent product danger.

Hycor Biomedical Inc vs all firms by recall-notice count

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

2 5031st 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 · 2026-09-15

Hycor Biomedical Inc in the notice-volume neighbourhood

Distinct federal recall events among this firm and nearest nationwide peers

notices

What this shows Hycor Biomedical 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 Aug 14, 2019

HYTEC 288 System, Model 74007P, automated immunoanalyzer (EIA) instrument. For in vitro diagnostic use only. HYTEC AUTOSTAT II RF assays: HYTEC AUTOSTAT II RF IgM Kit: Part Number FGA 05, HYTEC AUTOSTAT II RF IgA Kit: Part Number FGA 06, HYTEC AUTOSTAT II RF IgG Kit: Part Number FGA 07, HYTEC AUTOSTAT II Total Rheumatoid Factor Kit: Part Number FGA 08.
FDA Devices Moderate Aug 7, 2019

AUTOSTAT II IgM Rheumatoid Factor, IVD, Part: FGA 05 Product Usage: Rheumatoid Factor IgM ELISA is intended to be utilized as either a manual or an automated procedure The Intended Use is as follows: Enzyme-linked immunosorbent assay method for the semi-quantitative determination of specific IgM Rheumatoid Factor antibodies in human serum. The results of the IgM RF assay can be used as an aid in the diagnosis of Rheumatoid Arthritis when supported by other laboratory and clinical investigati

Hycor Biomedical 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 Hycor Biomedical Inc? ▼
PlainRecalls indexes 2 distinct federal recall events naming Hycor Biomedical 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 Hycor Biomedical Inc sit among other recalling firms? ▼
Hycor Biomedical Inc ranks #5,031 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 Hycor Biomedical Inc's notices? ▼
FDA Devices accounts for 2 of this firm's 2 indexed notices.
What product category dominates Hycor Biomedical Inc's filing book? ▼
Filings for Hycor Biomedical 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.
Hycor Biomedical 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 Hycor Biomedical Inc; individual notices remain authoritative on each linked recall page.

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