Cryo Cell International (CCEL) risk factors, FY2025 10-K

Cryo Cell International's FY2025 10-K, filed Feb 27, 2026, lists 41 risk factors in 6 groups. Against the prior year's 42: 1 new, 2 dropped, 4 substantially reworded.

Risk factors listed
416 groups
New this year
1vs 42 last year
Dropped
2since the prior 10-K
Substantially reworded
4of those kept
Section length
11k wordsItem 1A

What the changes say

  • The company added a delisting risk regarding NYSE American compliance.
  • Strategic spin-off risks and data security risks were reorganized.
  • Regulatory trial disclosures added capital raising constraints.

What changed since the prior 10-K

New

  • NewRisk Related to our Business

    Our common stock may be delisted from NYSE American LLC ("NYSE") if we fail to comply with continued listing standards

    Our common stock may be delisted from the NYSE American LLC if we fail to meet continued listing standards.

Dropped

  • DroppedRisk Related to our Business

    There is uncertainty with regard to whether we will be able to maximize shareholder value through the completion of a strategic transaction or successfully spinoff Celle Corp

    Uncertainty regarding maximizing shareholder value through strategic transactions or spinning off Celle Corp.

  • DroppedRisks Related to Information Technology

    or any significant breach of our data security could have an adverse effect on our business and may materially adversely affect our operating results and financial condition

Reworded

  • 77% rewrittenRisks Related to Information Technology

    If we experience a significant breach of data security or disruption in our information systems, our business could be adversely affected

    Added specific language stating that a significant data security breach could materially adversely affect operating results and financial condition.

  • 38% rewrittenRisk Related to our Business

    There is uncertainty with regard to whether we will be able to maximize shareholder value through the Duke License Agreement

    Removed references to the October 4, 2024 arbitration demand against Duke from the shareholder value risk heading and text.

  • 21% rewrittenRisk Related to our Business

    There is uncertainty with regard to the outcome of the Duke Arbitration Demand

    Updated financial statement note references from Note 18 to Notes 12 and 18 regarding the Duke Arbitration Demand.

  • 20% rewrittenRisk Related to our Business

    Our product candidates are subject to substantial government regulation, including the regulation of nonclinical testing and clinical trials. If we are unable to obtain regulatory approval for our product candidates, our ability to generate revenues related to such product candidate will be negatively impacted

    Removed COVID-19 pandemic restrictions and added an inability to raise sufficient capital as a reason for clinical trial delays.

All 41 risk factors

Headings as the filing states them, in filing order.

Risk Related to our Business

  1. 01Our common stock may be delisted from NYSE American LLC ("NYSE") if we fail to comply with continued listing standardsNew
  2. 02If we fail to meet any of the continued listing standards of the NYSE, our common stock could be delisted from the exchange. These continued listing standards include specifically enumerated criteria, including compliance with the NYSE's corporate governance requirements
  3. 03We may need to raise additional capital
  4. 04We may not be able to successfully grow or operate our business
  5. 05The Company’s operations and performance depend significantly on global and regional economic conditions
  6. 06Because our industry is subject to rapid technological and therapeutic changes and new developments, our future success will depend on the continued viability of the use of stem cells
  7. 07If our umbilical cord blood stem cell storage services do not achieve continued market acceptance, we will not be able to generate revenue necessary to support our business
  8. 08We may fail to successfully manufacture MSCs
  9. 09Clinical development is lengthy and uncertain
  10. 10Our product candidates are subject to substantial government regulation, including the regulation of nonclinical testing and clinical trials. If we are unable to obtain regulatory approval for our product candidates, our ability to generate revenues related to such product candidate will be negatively impacted20% rewritten
  11. 11lack of adequate funding to continue the clinical trial
  12. 12The stem cell preservation market is increasingly competitive
  13. 13A failure in the performance of our cryopreservation storage facility or systems, or those of Duke could harm our business and reputation
  14. 14Our future success depends on our ability to retain our key personnel and to attract, retain and motivate qualified personnel
  15. 15There is uncertainty with regard to the outcome of the Duke Arbitration Demand21% rewritten
  16. 16There is uncertainty with regard to whether we will be able to maximize shareholder value through the Duke License Agreement38% rewritten
  17. 17We are not assured of recouping our damages related to the Arbitration Demand against Duke nor our investment in the Duke License Agreement
  18. 18From time to time, the Company is subject to proceedings, lawsuits, contract disputes and other claims in the normal course of its business

Risk Related to Government Regulation

  1. 19If we do not obtain and maintain necessary domestic regulatory registrations, approvals and comply with ongoing regulations, we may not be able to market our services in the United States
  2. 20The final rule allows the FDA to inspect cord blood laboratories to determine compliance with the provisions of 21 CFR Part 1271. As part of this oversight authority, the FDA conducts unannounced inspections of cord blood banks
  3. 21Evolving legislation and regulations governing private cord blood banking in various jurisdictions throughout the world may impact the Company’s international licensees
  4. 22We may be required to spend substantial amounts to comply with legislative and regulatory initiatives relating to patient privacy
  5. 23Our failure to comply with laws related to hazardous materials could materially harm us

Risks Related to International Operations

  1. 24Our international operations are subject to risk and we may not be able to successfully protect our intellectual property
  2. 25We are subject to the Foreign Corrupt Practices Act
  3. 26The Company’s business may be impacted by political events, international trade disputes, war, terrorism, natural disasters, public health issues, industrial accidents and other business interruptions

Risks Related to Information Technology

  1. 27Our information systems are critical to our business, and a failure of those systems could materially harm us
  2. 28If we experience a significant breach of data security or disruption in our information systems, our business could be adversely affected77% rewritten
  3. 29Increasing use of social media could give rise to liability, breaches of data security, or reputational damage
  4. 30Some of our products contain open source software, which may pose particular risks to our proprietary software, technologies, products and services in a manner that could harm our business

Risks Related to Intellectual Property

  1. 31We may not be able to protect our intellectual property rights throughout the world
  2. 32We may become subject to third parties’ claims alleging infringement of their patents and proprietary rights, which could be costly, time consuming, and prevent the use of our technology solution

Risks Related to being a Public Company

  1. 33We incur significant costs and demands as a result of operating as a public company
  2. 34If we fail to maintain an effective system of internal control over financial reporting in the future, we may not be able to accurately report our financial condition, results of operations or cash flows, which may adversely affect investor confidence in us and, as a result, the value of our common stock
  3. 35Our disclosure controls and procedures may not prevent or detect all errors or acts of fraud
  4. 36Increasing scrutiny and changing expectations from investors, customers, and governments with respect to Environmental, Social and Governance (“ESG”) policies and practices may cause us to incur additional costs or expose us to additional risks
  5. 37significant control over matters subject to stockholder approval
  6. 38We may become subject to securities class action litigation, which can be expensive, divert management attention, and, if resolved unfavorably, expose us to significant liabilities
  7. 39We are a “smaller reporting company” and, as a result of the reduced disclosure and governance requirements applicable to smaller reporting companies, our common stock may be less attractive to investors
  8. 40We are responsible for the indemnification of our officers and directors
  9. 41Certain provision of our charter, bylaws and Delaware law may delay, defer or prevent a tender offer or takeover attempt that public stockholders might consider in their best interest

Other Cryo Cell International 10-Ks

  • FY2024 10-K risk factors
    42 risks

    Cryo-Cell International relies heavily on umbilical cord blood and tissue storage for revenue and faces risks related to clinical development, regulatory compliance, and a legal dispute with Duke University.

    Filed Feb 28, 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.