Product description
Mixtard 30/70 Innolet Human insulin 1001U/mL injection multidose cartridge, Batches NS63067 & NS63095. AUST R 75225.
See a list of details to help identify the product
Reason the product is recalled
Two batches of this product may have been exposed to frost during distribution to Western Australia. There is a possibility that the delivery mechanism may become jammed and unable to deliver insulin.
The hazards to consumers
Contamination.
What consumers should do
Consumers to return the product to the place of purchase.
Details to help identify the product
Supplier running the recall
Novo Nordisk Pharmaceuticals Pty Ltd
Identifying product features
(TGA R2004/1222)
Identifying numbers
Other identifying numbers
(TGA R2004/1222)
Where the product was sold
Western Australia
Responsible regulators
Regulators are established or appointed by government. They enforce regulations and rules.
Quote PRA number 2004/7255 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.