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539 result(s) found, displaying 176 to 200
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Market actionsRecall - potential medicine tampering
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Market actionsRecall - potential medicine tampering
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Market actionsHazard alert – risk of sudden loss of therapy due to reduced battery performance
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Market actionsHazard alert - increased risk of heart attack and blood clot
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Market actionsRecall for product correction - bottles supplied without child-resistant caps
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Market actionsRecall – potential failure to activate or need to apply increased force to activate
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Market actionsHazard alert due to potential for under-drainage.
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Market actionsHazard alert due to potential for MRI scans to affect valve positioning.
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Market actionsHazard alert due to increased risk of requiring revision.
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Market actionsRecall for product correction due to potential loss of therapy due to power error.
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Market actionsRecall due to risk of infection due to leakage.
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Market actionsHazard alert due to potential for partial loss of therapy.
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Market actionsHazard alert - higher than expected rate of PE inlay breakage
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Market actionsHazard alert due to revision rate increasing.
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Market actionsRecall for product correction - child-resistant caps may not function correctly
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Market actionsHazard alert due to potential for loss of telemetry and pacing due to battery malfunction.
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Market actionsRecall – potential for adverse events related to aristolochic acid(s)
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Market actionsHazard alert due to potential for implant failure due to loosening.
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Market actionsHazard alert due to risks of leaks, stent movement and aneurysm enlargement.
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Market actionsRecall for product correction due to risk of loss of therapy due to the recharger not functioning.
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Market actionsHazard alert due to higher-than-expected revision rate when used without patella resurfacing.