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1279 result(s) found, displaying 901 to 925
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Market actionsConsumers and health professionals are advised that LMT Surgical is issuing a hazard alert for all sizes and lots of its PyroTitan humeral resurfacing arthroplasty device.
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Safety alerts
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Market actionsIt has been identified that there is a potential for some screws from the affected lot to break during insertion or removal.
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Safety alertsHazard alert due to potential for breakage.
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Market actionsConsumers and health professionals are advised that Aimedics, in consultation with the TGA, is recalling from the market all units of its HypoMon sleep-time hypoglycaemic monitor.
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Market actionsZimmer is recalling from the market for the purpose of relabelling unused stock of its NexGen micro implants.
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Market actionsBoston Scientific has initiated a recall for product correction for multiple lots of its Promus Element Plus Monorail everolimus-eluting coronary stent system.
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Market actions
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Safety alerts
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Safety alerts
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Market actionsNovo Nordisk Pharmaceuticals has initiated a recall for product correction of certain lots of its NordiPen medical device.
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Market actionsStryker Australia has issued a hazard alert to surgeons regarding its Oasys Midline Occipital Plate.
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Market actionsRecall for product correction for Medtronic SynchroMed II and SynchroMed EL implantable infusion pumps.
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Safety alerts
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Safety alertsThe TGA warns that Plexus Slim Accelerator Capsules and the 3-Day Trial Pack are unsafe and illegal in Australia because they contain a banned substance that can cause serious health problems.
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Safety alerts
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Market actionsHealth professionals and consumers are advised that Medtronic Australasia is issuing a hazard alert for its Consulta Cardiac Resynchronization Therapy Pacemaker (CRT-P).
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Safety alertsHydroxyethyl starch (Voluven and Volulyte) and increased risk of mortality
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Market actionsGE Healthcare has initiated a recall for product correction for a number of its nuclear medicine imaging systems.
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Market actionsB. Braun Australia is withdrawing the cementless version of the Columbus Knee System from the Australian Register of Therapeutic Goods (ARTG). They have also issued a related hazard alert to surgeons.
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Safety alerts
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Market actionsSynthes Australia, in consultation with the TGA, is recalling unused stock of its 3.7 mm and 5.0 mm Dynamic Locking Screws.
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Safety alerts