Product description
Alpha Conducting Solution (ACS) 15mL used with Alpha-Stim M and AID devices
Manufactured between June 2014 and October 2018
Lot Numbers 081914-15, 111715-15, 070116-15, 020117-15, 080117-15, 010118-15, 041618-15, 071618-15, 102018-15
Alpha Conducting Solution Replacement (ACSR) 250mL used with Alpha-Stim M and AID devices
Manufactured between February 2014 and October 2018
Lot numbers 032014-25, 060515-25, 101615-25, 011716-25, 020117-25, 080117-25, 010118-25, 041618-25, 071618-25, 102018-25
ARTG 185395
(Pureplay Orthopaedics - gel, electrode)
Manufactured between June 2014 and October 2018
Lot Numbers 081914-15, 111715-15, 070116-15, 020117-15, 080117-15, 010118-15, 041618-15, 071618-15, 102018-15
Alpha Conducting Solution Replacement (ACSR) 250mL used with Alpha-Stim M and AID devices
Manufactured between February 2014 and October 2018
Lot numbers 032014-25, 060515-25, 101615-25, 011716-25, 020117-25, 080117-25, 010118-25, 041618-25, 071618-25, 102018-25
ARTG 185395
(Pureplay Orthopaedics - gel, electrode)
See a list of details to help identify the product.
Reason the product is recalled
The product may not effectively control microbial contamination.
The contamination, if present, will not be readily visible to the naked eye.
The contamination, if present, will not be readily visible to the naked eye.
The hazards to consumers
Microbial contamination may cause injury or illness.
What consumers should do
Consumers should immediately cease using the product and contact Pureplay to arrange a replacement product.
For more information, consumers should contact Pureplay Orthopaedics Customer Service on 03 9888 8808.
For more information, consumers should contact Pureplay Orthopaedics Customer Service on 03 9888 8808.
Details to help identify the product.
Supplier running the recall
Identifying numbers
Other identifying numbers
ACS Lot Numbers 081914-15, 111715-15, 070116-15, 02017-15, 080117-15, 010118-15, 041618-15, 071618-15, 102018-15 and ACSR Lot Numbers 032014-25, 060515-25, 101615-25, 011716-25, 020117-25, 080117-25, 010118-25, 041618-25, 071618-25, 102018-25
Where the product was sold
New South Wales
Queensland
South Australia
Tasmania
Victoria
Responsible regulators
Regulators are established or appointed by government. They enforce regulations and rules.
Quote PRA number 2019/17822 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.