*US FDA Recall data 2012 Onwards till date* - a Detailed Analysis is Ongoing to strengthen the Quality and applicable standard requirements. Soon Will be Published by Regulators and other statuary bodies. * So Far Medical Device Sector faced Lot of Quality Issues due to clarity and negligence. Since these data are managed by Only US, so Other Regulators are being intersted in evaluation to trace in thier jurisdiction. * Since India does not have trace mechanism for such data and issues so any quantiative analysis is not available till date.