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ARTICLE · 06 OCTOBER 2017

Medical Device Manufacturer's Duty To Warn

A recent decision of the Ontario Superior Court of Justice summarized the law in Canada concerning a medical device manufacturer's duty to warn in the context of class action litigation.

CanadaConsumer Protection

A recent decision of the Ontario Superior Court of Justice1 summarized the law in Canada concerning a medical device manufacturer's duty to warn in the context of class action litigation.

Product Liability Class Action

Typically the four steps in a products liability class action are: (1) determining whether the product is defective or whether, although non-defective, the product has a propensity to injure; (2) determining what the manufacturer knew about the dangerousness of its product; (3) given the state of the art and the extent of the risks inherent in the product's use, determining the reasonableness of the warning whether made directly to the consumer or to a learned intermediary; and (4) determining individual causation and damages. The first step, known as the general causation step, determines whether the product is capable of causing harm. The second step is part of determining whether the manufacturer had a duty of care not to sell the product or to

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