Market actions
Find significant or consumer level recalls, product alerts and product corrections.
Latest Market actions
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Key Sun Laboratories Pty Ltd is recalling four batches of lozenges due to the risk of a small metal wire being present in the lozenge.
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Aidacare Pty Ltd has updated the Instructions for Use (IFU) for the Aspire A205 Aluminium Patient Lifter. The IFU has been enhanced to strengthen existing instructions around correct and incorrect sling attachment methods and pre-use checks.
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Sanofi-Aventis Healthcare Pty Ltd T/A Sanofi Consumer Healthcare, is recalling the below products due to the potential presence of a glass fragment within the bottle (not within the tablets).
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Mindray Medical Australia Pty Ltd is conducting a product correction for the BeneHeart D1 Automated External Defibrillator. The operator’s manual is being updated for the procedure of switching patient types.
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AA-Med Pty Ltd is recalling two lots of Dexcom G7 sensors. These lots were identified for disposal and destruction in the USA due to incomplete sterilisation and deployment failure during testing.
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GlaxoSmithKline (GSK) Australia Pty Ltd is issuing a product correction for certain batches of their Flixotide and Pavtide Accuhalers as a small number of Accuhalers may not automatically reload the next dose.