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04 Jun 2003:
Recall of Pan Pharmaceuticals products

The Therapeutics Goods Administration (TGA), Australia has ordered the urgent recall of pharmaceutical products manufactured by Pan Pharmaceuticals Limited (Australia) and suspended its licence following a series of safety and quality breaches on 28 April 2003. The breaches included substitution of ingredients, manipulation of test results and substandard manufacturing processes.

Pan Pharmaceuticals represents 70% of the Australian complementary pharmaceutical market. It also does contract manufacturing for many other brands, some of which are available locally.


Actions taken by HSA

Due to the serious and widespread nature of the manufacturing problems identified by the TGA, HSA issued a press release on 28 April 2003 to advise the public to refrain from taking non-essential health products manufactured by Pan Pharmaceuticals.

To-date, 244 products marketed under 26 different brands in Singapore have been confirmed to be manufactured by Pan pharmaceuticals and all have been recalled from the market.


Other relevant information

The TGA was alerted to problems at Pan Pharmaceuticals in mid January 2003 when it started to receive serious ADR reports to Travelcalm®, an anti-motion sickness medicine manufactured by Pan Pharmaceuticals (this product is not available in Singapore). Subsequent inspections of Pan Pharmaceuticals manufacturing premises have since found evidence of widespread and serious deficiencies in the company's manufacturing and quality control procedures.

The Pan Pharmaceuticals products subjected to recall affect those manufactured since 1 May 2002 as this was the latest date that the TGA could ensure that Pan complied with the requirements of good manufacturing practices.


Public advisory

The products manufactured by Pan Pharmaceuticals for the Singapore market are non-prescription products and meant only for health supplementation. In addition, the TGA has informed HSA that there was no evidence of intentional adulteration of Pan Pharmaceuticals products with potent western drugs. To-date, no serious adverse drug reactions to these products have been reported locally.

Healthcare professionals are encouraged to report any suspected serious adverse drug reactions to vitamins and complementary medicines to the Pharmacovigilance (PV) Unit.


Last updated on 02 Jul 2010 16:55:15
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