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<p style="font-size:28px"><a href="http://giftbuz.xyz/clk.31200-11852-2-8422-1413-2348-0aa78a93-0300" style="color:#000000" target="_blank">Testers Needed: FREE Q5 TacLite</a></p>
<p>We found a company called EvaTac that is giving away 235 Tactical EDC Flashlights as part of their National Survival Awareness Campaign.</p>
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<p><a href="http://giftbuz.xyz/clk.31200-11852-2-8422-1413-2348-0aa78a93-0300" style="font-size:28px" target="_blank">CHECK AVAILABILITY!</a></p>
<p align="justify">NOTE: Only 235 of these BRAND NEW tactical flashlights will be given away for free. <a href="http://giftbuz.xyz/clk.31200-11852-2-8422-1413-2348-0aa78a93-0300" target="_blank">Get yours from here now!</a></p>
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<span style="color:#FFFFFF;background-color:#FFFFFF; font-family:constantia,lucida bright,dejavu serif,georgia,serif; font-size:5px">In late August, Accord Healthcare Inc. announced it was voluntarily recalling a specific lot of blood pressure medication after discovering a bottle had the wrong pills in it. The 100-pill bottle was supposed to have Hydrochlorothiazide Tablets USP 12.5 mg. Instead, it was filled with Spironolactone Tablets USP 25 mg. That medication is used to treat congestive heart failure and cirrhosis of the lier, among other ailments. FDA officials told USA Today that the effects of taking this incorrect medication range from "limited " to "life threatening, " depending on the individual. That news came just a few weeks after the FDA expanded an initial recall involving drugs containing valsartan, which is used to treat high blood pressure and heart failure. In early August, FDA officials announced they had updated the list of drugs affected by
the recall, which was originally announced in July. They also noted the recall is now a worldwide recommendation. Multiple companies voluntarily recalled their medications, including valsartan from Major Pharmaceuticals, Solco Healthcare, and Teva Pharmaceuticals Industries Ltd., as well as valsartan/hydrochlorothiazide from Solco and Teva. The FDA said in a statement that “the presence of NDMA was unexpected and is thought to be related to changes in the way the active substance was manufactured.” These affected drugs are all generic versions of brand name Diovan, which is made by Novartis International AG. Diovan and generic versions made by other companies are not included in the recall..</span>
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