Well, that is one long question. [laughter] I guess I don’t want to get too far into all of the details and tactics other than to say we obviously we were pleased with the outcome of no 483s in our two plants that have undergone that. And I’m not going to say we were pleased with the outcome in our distribution center, but if I said there’s good news, the good news is the distribution center, which doesn’t have all the technical nuances, clearly, that managing our plants do. So, as I think we indicated, and I indicated in my comments, we think we’ve really had our arms around where we need to get to, both as to, if you will, addressing the FDA, where we’re working with them. It’s not like we’re battling them. We’re moving forward. There is a tie-in with obviously our expectation to get Avaira Toric back out onto the market. Yes, it does take a special, or some type of filing, 510K, and we expect at this point in time, that we’ll be able to get back on the market by mid-fiscal year. So that is built into our assumptions, and keep in mind the plant in Puerto Rico makes both the Avaira Toric and all the high-volume Spheres, so the fact that we’ve been cleared on that side, that plant, and I don’t want to overstate what no comments means, relative to the regulatory process, but we factored where we think we are in the process into our guidance numbers and our expectation going forward. I think beyond that I really don’t want to get into a lot of nuances dealing with the recall, emphasizing that Avaira Toric was less than 1% of our revenue. It doesn’t warrant as much time and airtime as it’s been getting. And recognizing that even Avaira Sphere, which continues on the market, we swapped out, that represented less than 1% of our overall revenue. That was the issue of the partial recall. On the distribution side, I would just say, distribution side is packaging. If you can’t get that fixed, it’s kind of shame on you, so we’re not thinking we can’t be responsive at this juncture.