This product is being recalled, due to the detection of aristolochic acids by the Therapeutic Goods Administration Laboratories. Aristolochic acids have been associated with serious adverse reactions including severe kidney damage and urinary tract cancer.
Recall letters were dispatched today, 25 January 2002. Customers to be contacted via dispensing complementary healthcare practitioner.
Classification system:
Class I defects are potentially life-threatening or could cause a serious risk to health.
Class II defects could cause illness or mistreatment, but are not Class I.
Class III defects may not pose a significant hazard to health, but withdrawal may be initiated for other reasons.
Class I & II recalls are considered to be safety related recalls.
