Sonoma Pharmaceuticals (SNOA) risk factors, FY2026 10-K

Sonoma Pharmaceuticals's FY2026 10-K, filed Jun 16, 2026, lists 32 risk factors in 2 groups. Against the prior year's 32: 1 new, 1 dropped, 5 substantially reworded.

Risk factors listed
322 groups
New this year
1vs 32 last year
Dropped
1since the prior 10-K
Substantially reworded
5of those kept
Section length
9k wordsItem 1A

What the changes say

  • Product recalls, safety or efficacy allegations, mislabeling, and regulatory violations are newly highlighted as threats to sales and reputation.
  • Nasdaq’s proposed $5 million market-value requirement could create a faster suspension and delisting risk.
  • Outstanding options rose to 129,163 from 73,081, while shares available for future grants rose to 82,290 from 14,670.
  • Customer and receivables concentration shifted: customer C was 15% of revenue, while customers A and C were 12% and 19% of receivables.

What changed since the prior 10-K

New

  • NewRisks Related to Our Business

    Quality issues, concerns about safety or efficacy of our products, or failure to comply with governmental regulations could result in recall of our products and we could suffer adverse public relations that could adversely impact our sales, operating results, reputation and business operations

    Product quality, safety, efficacy, labeling, or regulatory problems could trigger recalls or withdrawals, damaging sales, reputation, and operations.

Dropped

  • DroppedRisks Related to Our Business

    We have a history of losses, we expect to continue to incur losses and we may never achieve profitability, and our March 31, 2025 audited consolidated financial statements included disclosure that casts substantial doubt regarding our ability to continue as a going concern

    Continuing losses, accumulated deficits, and substantial doubt about the company’s ability to continue as a going concern.

Reworded

  • 51% rewrittenRisks Related to Our Business

    If we fail to comply with the FDA’s rules and regulations and are subject to an FDA recall as part of an FDA enforcement action, the associated costs could have a material adverse effect on our business, financial position, results of operations and cash flows

    No substantive text changed; the risk continues to cover FDA enforcement, recalls, production shutdowns, and delayed or withdrawn product approvals.

  • 50% rewrittenRisks Related to Our Common Stock

    Our failure to maintain compliance with Nasdaq’s continued listing requirements could result in the delisting of our common stock

    Adds Nasdaq’s proposed $5 million market-value threshold, which could permit immediate suspension and delisting without a compliance period.

  • 31% rewrittenRisks Related to Our Common Stock

    Shares issuable upon the exercise of outstanding options may substantially increase the number of shares available for sale in the public market and depress the price of our common stock

    Options increased from 73,081 to 129,163, available grants from 14,670 to 82,290, and the risk now includes less favorable capital timing.

  • 23% rewrittenRisks Related to Our Business

    We rely on a number of key customers who may not consistently purchase our products in the future, and if we lose any one of these customers, our revenues may decline

    Current-year concentration changed to customer C at 15% of revenue; customer A is no longer listed for the current year.

  • 22% rewrittenRisks Related to Our Business

    Negative economic conditions increase the risk that we could suffer unrecoverable losses on our customers’ accounts receivable which would adversely affect our financial results

    Receivables concentration shifted from customer D at 24% to customers A at 12% and C at 19%.

All 32 risk factors

Headings as the filing states them, in filing order.

Risks Related to Our Business

  1. 01We depend on third party distributors and intend to continue to license or collaborate with third parties in various potential markets, and events involving these strategic partners or any future collaboration could delay or prevent us from developing or commercializing products
  2. 02We rely on a number of key customers who may not consistently purchase our products in the future, and if we lose any one of these customers, our revenues may decline23% rewritten
  3. 03A majority of our business is conducted outside of the United States, exposing us to additional risks that may not exist in the United States, which in turn could cause our business and operating results to suffer
  4. 04If we fail to obtain, or experience significant delays in obtaining, additional regulatory clearances or approvals to market our current or future products, we may be unable to commercialize these products
  5. 05If we fail to comply with ongoing regulatory requirements, or if we experience unanticipated problems with our products, these products could be subject to restrictions or withdrawal from the market
  6. 06Our products are classified as medical devices in the European Union (EU). In order to sell medical device products within the European Union, we are required to comply with the requirements of the Medical Devices Regulation, and its national implementations, including affixing CE markings on products
  7. 07If any of our third-party contractors fail to perform their responsibilities to comply with FDA rules and regulations, the manufacture, marketing and sales of our products could be delayed, which could decrease our revenues
  8. 08If we fail to comply with the FDA’s rules and regulations and are subject to an FDA recall as part of an FDA enforcement action, the associated costs could have a material adverse effect on our business, financial position, results of operations and cash flows51% rewritten
  9. 09Quality issues, concerns about safety or efficacy of our products, or failure to comply with governmental regulations could result in recall of our products and we could suffer adverse public relations that could adversely impact our sales, operating results, reputation and business operationsNew
  10. 10If our products do not gain market acceptance, our business will suffer because we might not be able to fund future operations
  11. 11If our competitors develop products with similar characteristics to our HOCl technology, we may need to modify or alter our business strategy, which may delay the achievement of our goals
  12. 12Negative economic conditions increase the risk that we could suffer unrecoverable losses on our customers’ accounts receivable which would adversely affect our financial results22% rewritten
  13. 13We may experience difficulties in manufacturing our products, which could prevent us from commercializing one or more of our products
  14. 14Our competitive position depends on our ability to protect our intellectual property and our proprietary technologies
  15. 15We may face intellectual property infringement claims that could be time-consuming, costly to defend and could result in our loss of significant rights and, in the case of patent infringement claims, the assessment of treble damages
  16. 16We could be required to indemnify third parties for alleged intellectual property infringement, which could cause us to incur significant costs
  17. 17We have significant international operations in Mexico and Europe, and we manufacture all of our products for export from Mexico. New or increased tariffs on goods imported into the United States, particularly tariffs on products manufactured in Mexico, could adversely affect our business
  18. 18Our sales in international markets subject us to foreign currency exchange and other risks and costs which could harm our business
  19. 19The markets in which we operate are highly competitive and subject to rapid technological change. If our competitors are better able to develop and market products that are less expensive or more effective than any products that we may develop, our commercial opportunity may be reduced or eliminated
  20. 20As a result, we may not be able to successfully commercialize any future products
  21. 21If we are unable to comply with broad and complex federal and state fraud and abuse laws, including state and federal anti-kickback laws, we could face substantial penalties and our products could be excluded from government healthcare programs
  22. 22We may not be able to maintain sufficient product liability insurance to cover claims against us
  23. 23Our ability to generate revenue will be diminished if our partners are unable to obtain acceptable prices or an adequate level of reimbursement from third-party payors, or our partners may face pricing pressure from private third-party payers, including customers, from rebates and restrictive reimbursement practices
  24. 24Our ability to generate revenue will be diminished if our partners are unable to manage customer product substitutions for our prescription products
  25. 25Our information technology and infrastructure may be breached or attacked, which could expose us to liability, damage our reputation, compromise our confidential information or otherwise adversely affect our business
  26. 26Our cash and cash equivalents may be exposed to failure of our banking institutions

Risks Related to Our Common Stock

  1. 27The market price of our common stock may be volatile, and the value of your investment could decline significantly
  2. 28Our operating results may fluctuate, which could cause our stock price to decrease
  3. 29Anti-takeover provisions in our certificate of incorporation and bylaws and under Delaware law may make it more difficult for stockholders to change our management and may also make a takeover difficult
  4. 30Our stockholders may experience substantial dilution in the value of their investment if we issue additional shares of our capital stock or other securities convertible into common stock
  5. 31Shares issuable upon the exercise of outstanding options may substantially increase the number of shares available for sale in the public market and depress the price of our common stock31% rewritten
  6. 32Our failure to maintain compliance with Nasdaq’s continued listing requirements could result in the delisting of our common stock50% rewritten

Other Sonoma Pharmaceuticals 10-Ks

  • FY2025 10-K risk factors
    32 risks

    Sonoma Pharmaceuticals relies heavily on international sales, particularly in Mexico and Europe, exposing it to foreign exchange, tariff, and credit risks. The company faces a going concern warning with an accumulated deficit of $197,806,000 as of March 31, 2025. Significant customer concentration exists, with customer B and customer C accounting for 21% and 18% of net revenues.

    Filed Jun 17, 2025

About this page

The headings are the filing's own. The one-line readings and the overview are automated and can be wrong: read Item 1A of the 10-K for the exact wording.