Product description

0.33g/Capsule
Brown Yellow Kuse

See a list of details to help identify the product

Reason the product is recalled

This product has been illegally supplied. The prescription-only (S4) medicine, Phentolamine, was detected in samples of the product. Schedule 4 medicines must only be used under medical supervision.

The hazards to consumers

Potentially life-threatening or could cause a serious risk to health (Class 1)

What consumers should do

Astrix Pty Ltd will contact affected consumers directly.

Details to help identify the product

Supplier running the recall

Astrix Pty Ltd

Identifying product features

N/A

Identifying numbers

Other identifying numbers

N/A

Where the product was sold

Nationally

Responsible regulators

Regulators are established or appointed by government. They enforce regulations and rules.

Quote PRA number 2008/10423 when contacting a regulator about this recall.

Recall and remedy questions

Contact the Therapeutic Goods Administration if you have:

  • a question about the remedy being offered to you by the business that is responsible for managing this recall, or
  • concerns about the way the business is managing this recall.