PRA number
Published date
Product description
DuoDERM Extra Thin and DuoDERM CGF adhesive wound dressings
Product codes: 187957, 187955 and 187660
Batches: 9J02859, 9H02226, 9H04865, 9L02456, 9L01731, 9L04890, 9K02656, 9H01234, 9M01779, 9H00183, 9B02984Y and 0A03460
ARTG 157331
(Convatec Australia Pty Ltd - Duoderm Extra Thin - Dressing, hydrogel)
ARTG 157332
(Convatec Australia Pty Ltd - Duoderm CGF - Dressing, hydrogel)
Reasons the product is recalled
The packaging of the adhesive wound dressings is not sealed together completely, leaving partial or fully open seals. The product may become non-sterile if the seal is open.
The hazards to consumers
If the dressing is non-sterile and used to treat wounds, this may result in infection and health complications.
What consumers should do
Consumers should not use the affected products and should contact ConvaTec Australia to arrange for the return of the products for a replacement or refund.
For more information, contact ConvaTec Australia by phone on 1800 339 412.
Supplier
Traders who sold this product
Hospitals, Pharmacies and Health Centres
Where the product was sold
Responsible regulator
Therapeutic Goods Administration is the responsible regulator for this recall.