Product liability law lets injured consumers seek compensation and pushes manufacturers to improve safety. Modern claims usually allege design defects, manufacturing defects, or failure to warn, and they interact with regulatory actions such as FDA or CPSC recalls. Cases can be lengthy; preserving the defective product, medical records, and acting quickly are essential.
Why product liability still matters
Product liability law keeps manufacturers accountable for dangerous goods. Over decades, regulators and lawsuits have removed harmful substances and unsafe products from the market - for example, the U.S. Environmental Protection Agency banned most uses of DDT in 1972 - and agencies such as the FDA, CPSC, and NHTSA now play active roles in recalls and post-market surveillance.
Lawsuits remain a consumer remedy when regulation, recalls, or warnings fail to prevent injury. They serve two roles: compensate injured people and create financial incentives for companies to design, test, and warn responsibly.
The common legal theories
Modern product liability claims typically rest on three theories:
- Design defect: the product's design is unreasonably dangerous when compared to its benefits or to reasonable alternative designs.
- Manufacturing defect: the product departs from its intended design and becomes dangerous during production.
- Failure to warn (marketing defect): the manufacturer did not provide adequate instructions or warnings about foreseeable risks.
Practical hurdles and legal limits
Product cases can be long and expensive. Plaintiffs must preserve evidence (the product, packaging, and medical records) and document how the product caused injury. Statutes of limitations and rules about comparative fault vary by state and affect recovery.
Some product lines face additional legal limits. For example, certain medical device and drug claims have been shaped by U.S. Supreme Court decisions and federal preemption doctrine, so remedies depend on whether federal regulation displaces state-law claims in a specific case.
How lawsuits, recalls, and regulation interact
Regulatory action (FDA recalls, CPSC hazard warnings, or NHTSA safety recalls) often accompanies litigation but does not automatically decide a private case. Companies may issue voluntary recalls to limit risk; regulators can order recalls or issue public safety notices when hazards emerge.
Class actions and mass-tort litigation are common where many people suffer similar injuries. These cases can streamline claims but vary in structure and outcomes.
Practical tips if you're injured by a product
- Preserve the product and packaging; photograph the scene and store the item safely.
- Get and keep medical records that link the injury to the product.
- Note dates, witnesses, and how you used the product.
- Contact an attorney with experience in product-liability or mass-tort cases quickly, because deadlines (statutes of limitations) are strict.