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Litigation Stage Tracker
Rapid GrowthEmerging
Formation
Active Litigation
Maturation
<45
45–55
55–70
70+
Talcum Powder (Cosmetic)
OpenFASTConsumer
500+
Total Cases
Causation
Plaintiffs allege cosmetic-grade talc is frequently contaminated with asbestos fibers due to geological co-occurrence of talc and asbestos deposits. Perineal application of talc-containing cosmetic powders enables asbestos fiber migration to the ovaries, causing chronic inflammation and malignant transformation. IARC classifies perineal talc use as 'possibly carcinogenic' (Group 2B). FDA testing in 2019-2020 found asbestos in multiple cosmetic products from various retailers.
Defendants
| Entity | Role | Note |
|---|---|---|
| Revlon Inc. | Manufacturer | Talc-containing cosmetic powders and foundations |
| Coty Inc. | Manufacturer | Cover Girl, Rimmel, and other talc-based cosmetics |
| Estee Lauder Companies | Manufacturer | MAC, Clinique, and other prestige cosmetic brands using talc |
| Colgate-Palmolive | Manufacturer | Cashmere Bouquet talc products |
| Imerys Talc America | Talc Supplier | Major talc mining and processing company — filed Chapter 11 |
Litigation Timeline
2006
IARC classifies perineal talc use as Group 2B — possibly carcinogenic
2019
FDA finds asbestos in Claire's and other retail cosmetic products
Feb 2020
Imerys Talc America files Chapter 11 bankruptcy
2023-2024
Lawsuits filed against non-J&J cosmetic talc manufacturers accelerate
2025
Plaintiff firms building inventory separate from J&J MDL
2026
~500 cases filed. MDL consolidation petition possible
Intelligence Signals
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Key Facts
- Status
- active
Geographic Exposure
·Various federal districts (Pre-MDL — no consolidation yet)
·New Jersey (significant filings — Imerys bankruptcy venue)
·Missouri (favorable plaintiff jurisdiction)
·California, Illinois (active filing states)
Eligibility Criteria
- ✓Used talc-containing cosmetic products (body powder, face powder, foundation)
- ✓Diagnosed with ovarian cancer
- ✓Regular use of talc products in perineal or genital area
- ✓Product was not manufactured by Johnson & Johnson (separate MDL 2738)