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§ 82.005.Design Defects

Title 4. Liability in Tort · Chapter 82. Products Liability · Last amended 1993 · Last verified August 29, 2026

In one sentenceSection 82.005 requires a design defect claimant to prove a safer alternative design that was economically and technologically feasible and would not substantially impair the product's utility.

Full Text of § 82.005

Text sizeJump to: (a) (b) (c) (d) (e)

(a)In a products liability action in which a claimant alleges a design defect, the burden is on the claimant to prove by a preponderance of the evidence that:
(1)there was a safer alternative design; and
(2)the defect was a producing cause of the personal injury, property damage, or death for which the claimant seeks recovery.
(b)In this section, "safer alternative design" means a product design other than the one actually used that in reasonable probability:
(1)would have prevented or significantly reduced the risk of the claimant's personal injury, property damage, or death without substantially impairing the product's utility; and
(2)was economically and technologically feasible at the time the product left the control of the manufacturer or seller by the application of existing or reasonably achievable scientific knowledge.
(c)This section does not supersede or modify any statute, regulation, or other law of this state or of the United States that relates to liability for, or to relief in the form of, abatement of nuisance, civil penalties, cleanup costs, cost recovery, an injunction, or restitution that arises from contamination or pollution of the environment.
(d)This section does not apply to:
(1)a cause of action based on a toxic or environmental tort as defined by Sections 33.013(c)(2) and (3); or
(2)a drug or device, as those terms are defined in the federal Food, Drug, and Cosmetic Act (21 U.S.C. Section 321).
(e)This section is not declarative, by implication or otherwise, of the common law with respect to any product and shall not be construed to restrict the courts of this state in developing the common law with respect to any product which is not subject to this section.
End

Plain-English Summary

The design defect elements, and the safer alternative design requirement is what makes these claims difficult.

The claimant must prove by a preponderance of the evidence that there was a safer alternative design and that the defect was a producing cause of the injury, damage, or death.

"Safer alternative design" is defined with four requirements built in. It means a design other than the one used that in reasonable probability: would have prevented or significantly reduced the risk without substantially impairing the product's utility; and was economically and technologically feasible at the time the product left the control of the manufacturer or seller by applying existing or reasonably achievable scientific knowledge.

The claimant must design the product. It is not enough to show the product was dangerous or that it failed — an alternative must be identified and shown to work, to preserve the product's usefulness, and to have been buildable and affordable at the time.

"At the time the product left the control of the manufacturer" excludes hindsight. A design that became feasible later does not establish the element.

Two exclusions. The section does not apply to a toxic or environmental tort as the proportionate responsibility chapter defines it, or to a drug or device as the federal Food, Drug, and Cosmetic Act defines those terms — pharmaceutical design claims are outside it.

Subsection (e) leaves the common law open: the section is not declarative of the common law and shall not be construed to restrict the courts in developing the common law with respect to any product not subject to this section.

Frequently Asked Questions

What must I prove for a design defect claim in Texas?

That a safer alternative design existed and that the defect was a producing cause of the injury.

What is a safer alternative design?

A different design that in reasonable probability would have prevented or significantly reduced the risk without substantially impairing the product's utility, and was economically and technologically feasible when the product left the manufacturer's control.

Does it apply to drugs?

No. The section excludes a drug or device as defined in the federal Food, Drug, and Cosmetic Act, and toxic or environmental torts.

Can I rely on later technology?

No. Feasibility is assessed at the time the product left the control of the manufacturer or seller.

Amendment History

  • Added by Acts 1993, 73rd Leg., ch. 5, Sec. 1, eff. Sept. 1, 1993.
Source & verification. Section text is reproduced verbatim from Texas Legislature Online (statutes.capitol.texas.gov). Enacted by the Texas Legislature. Current through May 14, 2026. Last verified August 29, 2026. · Official source