Folks, a word about recalls. Very often a recall is made for something as simple as a mistyped code on the label or poor packaging, failure to pass the quality assurance tests and such things. There might also be very minor variances in the manufacture of the device which, while it would not affect the user experience, was nevertheless, a variance and therefore not permitted. Such recalls are usually initiated by the firms themselves. Rarely are they made necessary by serious defects and certainly not by ones that are not found until after patients have had to have them revised.