Testosterone Therapy Lawsuit in Michigan

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People's Justice Legal Research Team
Filing Venue

Where to File in Michigan

Michigan TRT cases filed in federal court — including the E.D. Mich. or W.D. Mich. — are transferred to MDL 2545 in the Northern District of Illinois before Judge Matthew Kennelly. Michigan's large industrial male population in Detroit, Grand Rapids, Flint, and Lansing has contributed meaningful plaintiff numbers to MDL 2545. The MDL is largely resolved through global settlements with AbbVie, Endo, and Auxilium, but new Michigan cases involving AndroGel, Axiron, Androderm, Testim, or Fortesta cardiovascular injuries remain eligible for filing and review.

Michigan's statute of limitations for personal injury is three years under MCL § 600.5805(2), and for products liability also three years under MCL § 600.5805(13). Michigan applies the discovery rule, with limitations running from the time the plaintiff discovered or should have discovered the existence of the claim — including the causal link between TRT use and the cardiovascular injury. Michigan also has a product liability statute of repose that bars claims more than ten years after first sale of the product, which must be evaluated for cases involving TRT products purchased in the early 2000s.

Michigan has elevated rates of cardiovascular disease, particularly in the Detroit metro area and the industrial communities of Southeast Michigan. Michigan men in the 45–65 demographic showed high TRT prescription rates between 2010 and 2016, consistent with national trends. Henry Ford Health System, Beaumont Health, and Michigan Medicine treated a significant volume of TRT-associated cardiovascular events. Michigan's manufacturing workforce has historically elevated rates of hypertension, diabetes, and obesity — compounding cardiovascular risk from TRT products.

Michigan plaintiffs may file in Michigan Circuit Courts or in federal court. Michigan follows a modified comparative fault system and does not allow recovery if the plaintiff is more than 50% at fault. Michigan's product liability statute (MCL § 600.2945 et seq.) provides for strict liability in tort for design defect and failure-to-warn claims. Michigan also has a pharmaceutical liability exception that can limit failure-to-warn claims if the drug was approved by the FDA and adequate warnings were given to prescribing physicians — making pre-2015 FDA warning evidence especially critical in Michigan TRT cases.

FAQ

Frequently Asked Questions

The testosterone therapy (TRT) lawsuit involves men who used prescription testosterone products — including AndroGel, Axiron, Androderm, Testim, Fortesta, and Depo-Testosterone — and suffered serious cardiovascular injuries. Manufacturers allegedly marketed these products aggressively to men with normal age-related testosterone decline without adequate warnings about the risk of heart attack, stroke, and blood clots. The FDA issued a black box warning in 2015. Cases are consolidated in MDL 2545 in Chicago's federal court.
Key evidence includes: (1) prescription records or pharmacy records showing TRT use (AndroGel, Axiron, Androderm, etc.), (2) medical records documenting your cardiovascular injury — heart attack, stroke, DVT, or PE — including hospital records, discharge summaries, and test results, (3) timeline documentation showing TRT use preceded the cardiac event, and (4) records of any monitoring (or failure to monitor) hematocrit levels during TRT. An attorney can help obtain records through medical release authorization.
No. The testosterone therapy litigation is an MDL — multidistrict litigation — not a class action. MDL 2545 in Chicago's Northern District consolidated over 10,000 individual cases for pretrial coordination. Each plaintiff in MDL 2545 has their own individual case with individual compensation. The term 'class action' is sometimes mistakenly used in media coverage, but it is factually inaccurate for TRT litigation.
The MDL 2545 litigation includes: AndroGel 1% and 1.62% (AbbVie), Axiron (Eli Lilly), Androderm patch (Actavis/Allergan, now Teva), Depo-Testosterone injectable (Pfizer), Testim and Fortesta (originally Auxilium, later Endo Pharmaceuticals — now in bankruptcy), and Aveed (Endo). Generic testosterone products are also included. If you used any prescription testosterone product and suffered a cardiovascular injury, contact an attorney regardless of the specific brand.
You may qualify if you (1) used a prescription TRT product — including AndroGel, Axiron, Androderm, Testim, Fortesta, or Depo-Testosterone — for at least 30 days, and (2) were diagnosed with a heart attack, stroke, deep vein thrombosis (DVT), or pulmonary embolism (PE) during or within six months of TRT use, and (3) are within your state's statute of limitations (typically 2–3 years from the time you knew or should have known the injury was linked to TRT).
Settlement values in MDL 2545 vary by injury severity. Based on publicly reported data: DVT/PE cases without permanent injury have settled in the $15,000–$75,000 range; heart attack cases have ranged from $75,000 to $250,000+; stroke or permanently disabling cardiac events may reach $200,000–$600,000; wrongful death cases with strong facts have exceeded $500,000. AbbVie reportedly resolved its MDL inventory for an estimated $250M–$500M total (confidential). These figures are estimates only.
MDL 2545 — In re: Testosterone Replacement Therapy Products Liability Litigation — is the federal multidistrict litigation consolidating TRT personal injury cases in the U.S. District Court for the Northern District of Illinois in Chicago. Established in December 2014, it consolidated over 10,000 cases at its peak. MDL is not a class action — each plaintiff maintains an individual case. AbbVie's docket has largely been resolved; litigation against Eli Lilly (Axiron), Actavis/Teva (Androderm), and other defendants continues.
Yes. Statutes of limitations vary by state — most are 2–3 years from the date you knew or should have known your injury was linked to TRT. The 2015 FDA black box warning may trigger the discovery rule clock in some states. Filing a Short Form Complaint in MDL 2545 provides tolling protection for MDL inventory plaintiffs. Many attorneys recommend filing no later than 2 years from a cardiac event. If you used Testim or Fortesta (Endo products), bankruptcy trust claim deadlines apply — contact an attorney immediately.
AndroGel is a prescription testosterone gel manufactured by AbbVie Inc. and applied daily to the skin. At its peak, AndroGel generated over $1 billion in annual U.S. sales. AbbVie is accused of aggressively marketing AndroGel to men experiencing normal age-related testosterone decline — framing it as a treatable condition called "Low T" — without adequate disclosure of cardiovascular risks. AbbVie faced multiple bellwether trials in MDL 2545 and reportedly settled its global MDL docket for a confidential amount.
In March 2015, the FDA required all testosterone product manufacturers to add a black box warning — the agency's strongest safety label — specifically warning about the risk of venous thromboembolism (VTE), including deep vein thrombosis (DVT) and pulmonary embolism (PE). The FDA simultaneously restricted approved TRT uses to men with hypogonadism caused by specific underlying medical conditions, explicitly excluding normal age-related testosterone decline. A prior 2014 FDA communication had already flagged cardiovascular risk.
Yes, but the process is different. Endo Pharmaceuticals — which inherited Testim and Fortesta from Auxilium Pharmaceuticals — filed Chapter 11 bankruptcy in 2022. Claims against these products are now handled through Endo's bankruptcy trust, not through MDL 2545. Bankruptcy trust claim deadlines are set by the court and may differ significantly from standard statutes of limitations. If you used Testim or Fortesta, contact an attorney as soon as possible to protect your claim.
MDL (multidistrict litigation) is not a class action. In a class action, all plaintiffs share a single settlement regardless of individual injury. In MDL 2545, each plaintiff has their own individual case consolidated for pretrial purposes — including discovery and bellwether trials — but each receives individual compensation based on their specific injuries and damages. This distinction is important: in MDL, compensation reflects your personal injury severity, not a shared pot.
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