Tempus AI Sued for Sharing Genetic Data Worth $1.1B
Summary
Seven named plaintiffs from Illinois, California, New York, Michigan, Florida, Georgia, and West Virginia filed a federal class action lawsuit on April 15 against Tempus AI, alleging the company improperly obtained and shared genetic testing data from its $600 million acquisition of Ambry Genetics Corporation without patient notice or consent. The complaint alleges Tempus AI licensed the genetic data of more than one million individuals to over 70 pharmaceutical and biotech partners through agreements totaling more than $1.1 billion, using the data as AI training material. Illinois GIPA provides statutory damages of $15,000 per intentional or reckless violation or $2,500 per negligent violation, with potential class exposure reaching into the hundreds of thousands of members.
“Seven named plaintiffs from states across the country (Illinois, California, New York, Michigan, Florida, Georgia, and West Virginia) claim that they provided their genetic information to Ambry Genetics Corporation for medical testing purposes with the expectation that it would be kept confidential.”
Healthcare organizations and employers that have licensed AI-powered diagnostic, research, or clinical decision-support tools should proactively review their vendor agreements for data consent, de-identification, and downstream use representations. Plaintiffs' attorneys have previously used vendor websites, press releases, and earnings calls to identify downstream customers in similar privacy litigation waves, arguing that customers either knew or should have known about potential legal exposure of the platforms they deployed.
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What changed
The lawsuit alleges Tempus AI violated multiple state genetic privacy statutes including Illinois's Genetic Information Privacy Act (GIPA), California's Confidentiality of Medical Information Act, and consumer protection laws across seven states, along with common law claims for negligence, unjust enrichment, fraudulent concealment, conversion, invasion of privacy, breach of contract, and breach of fiduciary duty. Healthcare organizations and MedTech companies that license AI-powered diagnostic, research, or clinical decision-support tools may face downstream litigation exposure as named defendants simply by virtue of being known customers of platforms trained on patient data without verified consent. Companies should audit their AI vendor relationships, review vendor contracts for data consent and indemnification provisions, and monitor state-specific genetic or health data privacy obligations.
Archived snapshot
Apr 24, 2026GovPing captured this document from the original source. If the source has since changed or been removed, this is the text as it existed at that time.
April 23, 2026
AI Company’s Acquisition of Genetic Testing Firm Sparks Landmark Privacy Lawsuit – What Employers and MedTech Should Know
James Fessenden, Danielle Kays Fisher Phillips + Follow Contact LinkedIn Facebook X ;) Embed
A recent Illinois federal class action lawsuit alleges an AI healthcare company obtained health data during a corporate acquisition and shared that data with biotech and pharmaceutical companies in violation of key privacy laws. MedTech companies and their business customers should pay attention. The April 15 lawsuit targets Tempus AI, a Chicago-based healthcare technology company, and stems from its February 2025 acquisition of a genetic testing firm with a database of more than one million genetic tests. The plaintiffs allege that Tempus AI compelled the acquired firm to hand over its entire cache of genetic testing data shortly after the acquisition and then licensed their data to more than 70 pharmaceutical and biotech partners through agreements totaling more than $1.1 billion, all without providing notice, much less obtaining the written consent of the patients. What do employers and MedTech companies need to know about this new avenue of attack we’ll likely be seeing more of in the near future?
What the Lawsuit Alleges
Seven named plaintiffs from states across the country (Illinois, California, New York, Michigan, Florida, Georgia, and West Virginia) claim that they provided their genetic information to Ambry Genetics Corporation for medical testing purposes with the expectation that it would be kept confidential. When Tempus AI completed its $600 million acquisition of Ambry, the suit alleges, their data was swept up and transferred without notice or consent, then commercially exploited as training data for Tempus AI’s artificial intelligence tools and as a licensed dataset for third-party life sciences companies.
| Important caveat: These are simply allegations in a civil complaint. Tempus AI has not yet had the opportunity to respond, and nothing in this lawsuit has been proven in court. The company may have defenses (legal, factual, or both) that have not yet been presented, so read this summary with a grain of salt. |
The complaint alleges Tempus AI’s revenue grew more than 83% year-over-year in 2025, and attributes much of that growth to the commercialization of the Ambry genetic data. The plaintiffs further allege that Tempus AI’s public statements that it only shares “de-identified” data don’t hold up. They argue genetic data is inherently identifiable and cannot be meaningfully anonymized, regardless of what labels are stripped away.
The legal claims span a wide range of state statutes: Illinois’s Genetic Information Privacy Act (GIPA), the California Confidentiality of Medical Information Act, and consumer protection laws in Florida, Georgia, Michigan, New York, and West Virginia. The complaint also includes common law claims for negligence, unjust enrichment, fraudulent concealment, conversion, invasion of privacy, breach of contract, and breach of fiduciary duty.
The Genetic Data Angle
What makes this case particularly consequential is the nature of the data involved. Genetic information occupies a uniquely sensitive category under the law. Plaintiffs allege Congress recognized that when it passed the Genetic Information Nondiscrimination Act (GINA) in 2008. Unlike a Social Security number that can be changed or a password that can be reset, your DNA is permanent, deeply personal, and predictive of health conditions that extend to your biological relatives. More than a dozen states have enacted additional genetic privacy protections since then.
Illinois’s GIPA, the lead statute in this case, is among the most stringent. It requires written authorization before genetic testing results can be disclosed to anyone other than the tested individual. The statute provides for statutory damages of $15,000 per intentional or reckless violation, or $2,500 per negligent violation. With a class potentially numbering in the hundreds of thousands, the exposure in a case like this may be staggering.
Why This Case Could Be an Inflection Point
If you’ve been following AI-related privacy litigation over the past two years, this case might look familiar. The pattern mirrors what we saw with AI call recording and transcription services: lawsuits against the platform developers came first, followed quickly by suits against their enterprise customers: the companies that purchased and deployed those tools.
The Tempus AI complaint is notable because the company serves major healthcare systems, research institutions, and life sciences companies, and it has publicly touted the breadth of its data-sharing partnerships. In prior litigation waves, plaintiffs’ attorneys have used vendor websites, press releases, and earnings calls to identify downstream customers, arguing that those customers either knew or should have known that the platforms they were using had legal exposure.
Healthcare and MedTech companies that license AI-powered diagnostic, research, or clinical decision-support tools may be drawn into litigation as a named defendant simply by virtue of being a known customer.
4 Things Employers and MedTech Companies Should Do Now
- First, audit your AI vendor relationships. If your organization uses any AI-powered health, diagnostics, or research tool, find out exactly what data is flowing through it and where it goes, including whether that data is used to train models or licensed to third parties.
- Second, review your vendor contracts. Does your agreement with the platform provider include representations about data consent, de-identification, and downstream use? What data can vendors’ employees access? Are there indemnification provisions that would protect your organization if the vendor’s practices are later found to be unlawful?
- Third, know your state law obligations. Plaintiffs’ counsel deliberately assembled a nationwide class that maps to different state privacy regimes. If you operate in California, Illinois, New York, or other states with robust genetic or health data privacy laws, you are at higher risk and have a greater obligation to stay up to speed on local requirements.
Fourth, monitor the litigation. If this case proceeds to class certification and survives early motions, expect a wave of similar suits targeting not just platform developers but healthcare employers and MedTech companies that incorporated AI tools trained on patient data without verified consent.
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DISCLAIMER: Because of the generality of this update, the information provided herein may not be applicable in all situations and should not be acted upon without specific legal advice based on particular situations.
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