PlainRecalls

OraSure Technologies, Inc.

10 recalls on record · Latest: Mar 17, 2021

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Agency notice ledger

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

#1,501 of 14,151 · 10 notices · 0.010% archive

  • BOOK 10 notices
  • RANK #1,501 of 14,151
  • SHARE 0.010% archive
  • AGENCY FDA Devices (10)
  • CAT medical devices
  • CATS 1 category
  • LATEST Mar 17, 2021
  • PHOTO 4 Earth Farms formerl…

Nearest notice-volume peer: 4 Earth Farms formerly Mcl Fresh Inc (0 notice gap)

OraSure Technologies, Inc. accounts for about 0.010% of the 104,423-notice archive on 10 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 OraSure Technologies, Inc. sits among 14,151 recalling firms

OraSure Technologies, Inc. ranks 1,501st of 14,151 tracked firms by distinct recall-event count. Archive size reflects filing volume, not inherent product danger.

OraSure Technologies, Inc. vs all firms by recall-notice count

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

10 1501st of 14151 higher than 12,602 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

OraSure Technologies, Inc. in the notice-volume neighbourhood

Distinct federal recall events among this firm and nearest nationwide peers

notices

What this shows OraSure Technologies, Inc. holds about 0.010% of archive notices alongside 10 distinct filings.

Source FDA · CPSC · USDA FSIS · NHTSA filings aggregated by PlainRecalls As of September 2026
FDA Devices Low Mar 17, 2021

Methamphetamine Intercept Microplate kit EIA - IVD qualitative determination of methamphetamine in oral fluid, PN 11041C.

FDA Devices Low Sep 30, 2020

Pointts sistema de ellmlnact!;o de verrugas OTC - Brazil Catalog Number: 1001-0280 - Product Usage: indicated for over-the-counter a cryosurgical system for the treatment of skin tags.

FDA Devices Low Sep 30, 2020

Personelle OTC Skin Tag Remover, Canada Catalog Number: 1001-0314 - Product Usage: indicated for over-the-counter a cryosurgical system for the treatment of skin tags.

FDA Devices Low Sep 30, 2020

CVS Advanced Wart Remover Kit, Catalog Number: 1001-0407 - Product Usage: indicated for over-the-counter a cryosurgical system for the treatment of common warts and plantar warts.

FDA Devices Low Sep 2, 2020

Orasure Technologies Interept Benzodiazopene Miro-Plate EIA-Benzo EIA 2 plate Matrix Oral Fluid Coated Micro-Plate. IVD Immunoassay for Benzodiazepines, Product Number: 1110IT

FDA Devices Low Sep 2, 2020

Orasure Technologies Interept Benzodiazopene Miro-Plate EIA-Benzo EIA 5plate Matrix Oral Fluid Coated Micro-Plate-IVD Immunoassay for Benzodiazepines, Product Number: 1110IB

FDA Devices Low Apr 25, 2018

Cocaine Metabolite MICRO-PLATE EIA, Catalog Number: 1122SC, UDI: (0100608337000429(17)180228(10)000

FDA Devices Low Dec 14, 2016

Barbiturates Intercept Micro-Plate EIA (enzyme immunoassay, barbiturate) Product is intended for use by clinical laboratories in the qualitative determination of barbiturates in oral fluids.

FDA Devices Critical Aug 24, 2016

OraQuick Ebola Rapid Antigen Test, Product Code 3001-2807; Intended for the qualitative detection of antigens for Ebola viruses.

FDA Devices Low Apr 27, 2016

OraQuick HCV Visual Reference Panel Intended to assist new operation in becoming proficient at reading specimens with antibody levels near the limit of detection of the device.

OraSure Technologies, Inc. holds a measurable archive slice

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 OraSure Technologies, Inc.?
PlainRecalls indexes 10 distinct federal recall events naming OraSure Technologies, 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 OraSure Technologies, Inc. sit among other recalling firms?
OraSure Technologies, Inc. ranks #1,501 of 14,151 by distinct recall-event count among 14,151 firms in this archive (89th percentile of firms with fewer notices). Rank tracks filing frequency, not product danger.
Which agency issues most of OraSure Technologies, Inc.'s notices?
FDA Devices accounts for 10 of this firm's 10 indexed notices.
What product category dominates OraSure Technologies, Inc.'s filing book?
Filings for OraSure Technologies, 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.
OraSure Technologies, Inc.: 10 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 OraSure Technologies, Inc.; individual notices remain authoritative on each linked recall page.

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