For nearly 40 years federal food safety regulators had prohibited the use of any part of the cow heart in making ground beef. With little fanfare, that policy has changed. [More]
Over the past few years, Southwest Airlines has undergone quite a corporate metamorphosis: completing the purchase of AirTran and beginning operation of its first international flights. But no transformation is complete without the big makeover reveal scene (at least that’s the formula in every teenage chick-flick I ever saw). Southwest’s time on the runway came today as the company debuted a new look. [More]
As is custom for Valentine’s Day, many businesses are offering heart-shaped merchandise. Papa John’s Pizza is offering a such a themed pizza. But, as is often the case, reality can be strikingly different than advertising. Come inside to see what the pizza actually looks like.
Last time I checked, an adult male should consume 2,500 calories a day, and this shake nearly meets that requirement! The saturated fat present in that shake is over 3 times the RDA of 20 grams, which will put you on the fast track for heart disease. Of course, that’s if the Type 2 diabetes caused by all 266 grams of that sugar doesn’t get you first.
Medtronic is “recalling” its latest heart defibrillator models because of faulty wiring, which could lead to either it not working when you most need it, or it shocking you randomly in the heart with painful electric jolts. “The company is urging all of the roughly 235,000 patients with the lead, known as the Sprint Fidelis, to see their doctors to make sure it has not developed a fracture that can make the device misread heart-rhythm data.”
The FDA has launched a safety review of the heartburn drugs Prilosec and Nexium after two studies linked the medicines to an increased risk of: “heart attacks, heart failure, and heart-related sudden death.” The FDA warned that the studies are only preliminary, and that doctors and patients should keep using the drugs. From the LA Times:
The Food and Drug Administration has warned Guidant that, in the agency’s opinion, it has not resolved the manufacturing problems detected in an earlier inspection. In a letter to the company, the FDA said that would likely result in restrictions on its ability to bring new heart devices to the market…