Australia

A medical device implanted in me was later recalled due to defects. Can I claim damages?

6 years
Limitation period
$100k+
Compensation cap
ACL s. 54
Consumer guarantee
s. 138
Strict liability
The Short Answer

Yes, you may be able to claim damages under the Australian Consumer Law if the implanted medical device was unsafe, defective, or failed to meet consumer guarantees.

What the Law Says

The Australian Consumer Law (ACL), which forms part of the Competition and Consumer Act 2010, provides rights and remedies when goods—including medical devices—are unsafe or defective.

Medical devices implanted in patients are considered 'goods' under the ACL. If a device is found to be defective and causes injury, you may have a claim for compensation under strict liability provisions.

Section 138 of the Competition and Consumer Act 2010 (Cth) imposes strict liability on manufacturers for injuries caused by defective goods. This means you do not need to prove negligence — only that the device was defective and caused harm.

The ACL also includes consumer guarantees under Division 1 of Part 3-2. Section 54 guarantees that goods are of acceptable quality, including being safe and free from defects. A recalled implant strongly suggests it failed this guarantee.

You generally have up to 6 years from the date of injury (or when you reasonably discovered it) to bring a claim under the ACL, though state limitation statutes may apply depending on the cause of action.

Statutory Text

A manufacturer of goods is liable to compensate a person who suffers loss or damage because of a safety defect in the goods supplied by the manufacturer.

Competition and Consumer Act 2010 (Cth), s. 138 — Liability of manufacturers for defective goods
Statutory Text

Goods are of acceptable quality if they are safe, durable and free from defects...

Competition and Consumer Act 2010 (Cth), s. 54 — Guarantee as to acceptable quality

What to Do

1

Contact your treating doctor and obtain full medical records related to the implant and any complications.

2

Report the issue to the Therapeutic Goods Administration (TGA) via their adverse event reporting system.

3

Seek legal advice promptly — time limits apply, and evidence collection is critical.

4

Gather documentation: implant identification details, recall notice, surgical reports, and proof of expenses or lost income.

Sources

Same Question, Other Jurisdictions

Not legal advice. This article is general information based on publicly available sources, written for educational purposes. Laws change and individual situations vary. Consult a licensed attorney in your jurisdiction before acting on anything you read here. Last reviewed: 2026-06-08.