FDA Ends Emergency Use for Three Old COVID Tests
Published Date: 6/26/2026
Notice
Summary
The FDA has officially ended emergency use for three COVID-19 test kits from BD, InBios, and Roche as of early 2026. This means these specific tests are no longer authorized for quick COVID-19 detection or diagnosis. If you or your organization used these tests, it’s time to switch to other approved options—no extra costs or penalties, just a smooth transition.
Analyzed Economic Effects
3 provisions identified: 0 benefits, 3 costs, 0 mixed.
BD Veritor EUA Revoked Feb 24, 2026
FDA revoked the Emergency Use Authorization (EUA) for the BD Veritor System for Rapid Detection of SARS-CoV-2 effective February 24, 2026. BD requested the revocation, told FDA there are no viable BD Veritor reagents remaining in U.S. distribution, and has transitioned to a cleared BD Veritor product under K243872; the revoked EUA device is no longer authorized for emergency COVID-19 detection or diagnosis.
InBios SCoV-2 Detect EUA Revoked Feb 24, 2026
FDA revoked the Emergency Use Authorization (EUA) for InBios International, Inc.'s SCoV-2 Detect Neutralizing Ab ELISA effective February 24, 2026. InBios requested the revocation and stated there are no viable SCoV-2 Detect Neutralizing Ab ELISA reagents remaining in U.S. distribution; the revoked EUA device is no longer authorized for emergency COVID-19 detection or diagnosis.
Roche Elecsys EUA Revoked March 2, 2026
FDA revoked the Emergency Use Authorization (EUA) for Roche Diagnostics' Elecsys Anti-SARS-CoV-2 effective March 2, 2026. Roche requested the revocation, indicated there are no viable Elecsys reagents remaining in U.S. distribution, and has transitioned to a cleared Elecsys product under K250768; the revoked EUA device is no longer authorized for emergency COVID-19 detection or diagnosis.
Personalized for You
How does this regulation affect your finances?
Personalize government policy and PRIA will tell you what this federal register document means for your household, plus every other regulation we track. PRIA reads each provision against your financial profile to show you exactly what matters to your wallet.
Key Dates
Department and Agencies
Related Federal Register Documents
2026-14073, Drug Establishment Registration and Drug Listing Requirements for Establishments Engaged in Distributed Manufacturing and Certain Foreign Establishments
The FDA wants to make it easier for drug makers who work in several locations to register as one company instead of many. They’re also updating rules for foreign drug companies to match new laws about handling health threats. If you’re in drug manufacturing, get ready to comment by September 11, 2026, and keep an eye on possible paperwork changes that could affect your business.
2026-13047, Establishment Registration and Product Listing for Tobacco Products
The FDA wants to make sure all tobacco product makers, both in the U.S. and abroad, register their businesses and list their products. This new rule closes a big gap by including foreign companies, helping the FDA keep better track of tobacco products for public health. Comments on this proposal are open until September 14, 2026, so affected businesses should get ready to update their info and possibly face new costs.
2026-15920, Micro-Tracers, Inc.; Response to Objections and Requests for a Public Hearing
The Food and Drug Administration (FDA or we) received objections and requests for a public hearing submitted by Buchanan Ingersoll & Rooney PC, on behalf of Micro-Tracers, Inc. (Micro-Tracers or objector), on the order granting a color additive petition (3C0323) requesting that we repeal specified regulations to no longer provide for the safe use of FD&C Red No. 3 in food (including dietary supplements) and ingested drugs. After reviewing the objections, we have concluded that the objections do not raise issues of material fact that justify a hearing. We are also providing notice that the administrative stay of the effective date for the repeal and delisting of the color additive regulations is now lifted.
2026-15613, Assessing Adhesion With Transdermal and Topical Delivery Systems for ANDAs; Guidance for Industry; Availability
The Food and Drug Administration (FDA or Agency) is announcing the availability of a final guidance for industry titled "Assessing Adhesion With Transdermal and Topical Delivery Systems for ANDAs." This guidance provides recommendations for the design and conduct of studies evaluating the adhesion performance of a transdermal or topical delivery system (collectively referred to as TDS). Depending on the objectives of a generic TDS product development program, applicants may choose to evaluate TDS adhesion in studies performed to evaluate TDS adhesion only, or in studies performed with a combined purpose (e.g., for the simultaneous evaluation of adhesion and bioequivalence (BE) with pharmacokinetic (PK) endpoints). The recommendations in this guidance relate to studies submitted in support of an abbreviated new drug application (ANDA). The guidance replaces the draft guidance (Revision 2) "Assessing Adhesion With Transdermal and Topical Delivery Systems for ANDAs," issued on April 13, 2023.
2026-15635, Angela Anatilde Baquero: Final Debarment Order
The Food and Drug Administration (FDA or the Agency) is issuing an order under the Federal Food, Drug, and Cosmetic Act (FD&C Act) permanently debarring Angela Anatilde Baquero from providing services in any capacity to a person that has an approved or pending drug product application. FDA bases this order on a finding that Angela Anatilde Baquero was convicted of a felony under Federal law for conduct relating to the development or approval, including the process for development or approval, of any drug product. Mrs. Baquero was given notice of the proposed debarment and an opportunity to request a hearing within the timeframe prescribed by regulation. As of May 6, 2026 (30 days after receipt of the notice), Mrs. Baquero has not responded. Mrs. Baquero's failure to respond and request a hearing constitutes a waiver of Mrs. Baquero's right to a hearing concerning this matter.
2026-15612, Assessing the Irritation and Sensitization Potential of Transdermal and Topical Delivery Systems for ANDAs; Revised Draft Guidance for Industry; Availability
The Food and Drug Administration (FDA or Agency) is announcing the availability of a revised draft guidance for industry titled "Assessing the Irritation and Sensitization Potential of Transdermal and Topical Delivery Systems for ANDAs." This revised draft guidance provides recommendations for the design and conduct of studies to evaluate the in vivo skin irritation (and sensitization, if applicable) potential of a proposed transdermal or topical delivery system (collectively referred to as TDS). The recommendations in this revised draft guidance relate to studies submitted in support of an abbreviated new drug application (ANDA). The revised draft guidance is intended to clarify FDA's recommendations and expectations related to in vivo skin irritation and in vivo combined skin irritation and sensitization studies. This draft guidance replaces the draft guidance "Assessing the Irritation and Sensitization Potential of Transdermal and Topical Delivery Systems for ANDAs" (April 2023).
Previous / Next Documents
Previous: 2026-12893, Combined Notice of Filings #1
Big energy players like Southwestern Electric Power and Appalachian Power are making moves to take over wind energy projects, which could shake up how electricity is generated and managed. The Federal Energy Regulatory Commission is reviewing these changes and some rate updates that might affect costs starting June 1, 2026. If you want to weigh in, comments are due by July 13, 2026, so don’t miss your chance!
Next: 2026-12907, Evaluation of the California Coastal Management Program; Notice of Public Meetings; Request for Comments
NOAA is checking in on California’s Coastal Management Program and wants your thoughts! They’re hosting one in-person meeting and two online meetings in August 2026 to hear from folks about spaceports, oil, pipelines, desalination, and undersea cables. If you care about California’s coast, now’s the time to speak up before the August 22 deadline—no money changes yet, just your chance to shape the future!