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536 result(s) found, displaying 176 to 200
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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 - increased risk of requiring revision
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Market actionsHazard alert - potential for MRI scans to affect valve positioning
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Market actionsRecall for product correction - potential loss of therapy due to power error
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Market actionsRecall – risk of infection due to leakage
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Market actionsHazard alert - potential for partial loss of therapy
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Market actionsHazard alert - revision rate increasing
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Market actionsHazard alert - higher than expected rate of PE inlay breakage
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Market actionsRecall for product correction - child-resistant caps may not function correctly
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Market actionsHazard alert - 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 - potential for implant failure due to loosening
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Market actionsHazard alert - risks of leaks, stent movement and aneurysm enlargement
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Market actionsRecall for product correction - risk of loss of therapy due to the recharger not functioning
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Market actionsHazard alert - higher than expected revision rate when used without patella resurfacing
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Market actionsHazard alert - risk of premature battery depletion
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Market actionsRecall for product correction - risk of injury due to D-clip becoming damaged
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