Medical device recall refers to the behavior of medical device manufacturers to eliminate defects by warning, inspection, repair, re labeling, modifying and improving instructions, software upgrading, replacement, recovery, destruction and other means according to the prescribed procedures for a certain category, model or batch of products with defects that have been sold on the market. Defect refers to the unreasonable risk that medical devices may endanger human health and life safety under normal use.
Post time: Dec-10-2021