Shen Neng Herbal Medicines Group - Jin Gui Shen Qi Wan (Oral Pills) Recall

A recall notice for Jin Gui Shen Qi Wan (Oral Pills) supplied by Shen Neng Herbal Medicines Group Pty Ltd.

Shen Neng Herbal Medicines Group Pty Ltd — Jin Gui Shen Qi Wan (Oral Pills)



Date published

8 Sep 2019

Product description

Jin Gui Shen Qi Wan (Oral Pills)

A complementary medicine used in traditional Chinese medicine, marketed to help or treat various complaints including mild bronchitis

All Batches

ARTG 217716

Photograph of Jin Qui Shen Qi Wan Pills|250x308

Identifying features


AUST L 217716

What are the defects?

The product contains levels of aconitum alkaloids that are higher than the limit permitted for a listed medicine. These substances can pose an unacceptable risk to human health.

The product label does not restrict the medicine’s use to adults.

What are the hazards?

Potential risk of aconitum alkaloid poisoning, which may damage the heart, nervous system and gastrointestinal system.

Children are particularly at risk, as toxicity can occur at normal doses. An accidental overdose could be fatal in a small child.

What should consumers do?

Consumers should immediately stop using this product and return it to the place of purchase for a full refund.

Potential signs or symptoms of aconitum alkaloids poisoning include:

  • low blood pressure, palpitations, chest pain, abnormal heart rhythm
  • tingling or numbness in the face or limbs, muscle weakness
  • nausea, vomiting, abdominal pain, diarrhoea.

If you have taken Jin Gui Shen Qi Wan pills and experience any of the above symptoms, seek medical attention or call the Poisons Information Centre on 13 11 26. If you have any questions or concerns about this issue, talk to your health professional.

See for a Chinese translation of the recall information.

For further information, consumers can contact Shen Neng Herbal Medicines Group on 02 9416 9831.


Shen Neng Herbal Medicines Group Pty Ltd

Traders who sold this product

Chinese Medicine Clinics

Where the product was sold

Australian Capital Territory

New South Wales


South Australia


Western Australia

Responsible regulator

Therapeutic Goods Administration is the responsible regulator for this recall.

Product category