Medtronic’s voluntary recalled for the affected products unit, distributed worldwide marked as major restraining factor
Maintaining the product quality is essential to avoid product recalls. Medtronic’s voluntary recalled many pipelines embolization devices, such as Alligator retrieval device, Ultraflow, marathon flow directed micro catheters, and X-celerator hydrophilic guidewire. This recall was conducted worldwide in 2016, due to potential separation and detachment of polytetrafluoroethylene (PTFE) coating on the parts of flow directed micro catheters.
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