Nine surgical mesh products have been removed from supply in New Zealand after recent regulatory action by Medsafe to check the products' safety.
Medsafe decided to ban the supply of the mesh for operations such as pelvic organ prolapse and stress urinary incontinence after the Australian Therapeutic Goods Administration (TGA) reviewed surgical mesh for urogynaecological use, and took regulatory action.
ACC figures also showed that the mesh had cost at least $13 million in injury payouts in the past 12 years.
In December 2017, Medsafe used the provisions in the Medicines Act 1981 to request safety information from four suppliers of surgical mesh products in New Zealand.
The companies included Boston Scientific NZ Ltd, Culpan Medical, Endotherapeutics NZ Ltd and Johnson & Johnson Medical NZ.