Food Safety Quiz From The FDA
4 years ago
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- 4 years ago
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Please oppose Bill 5-10, 'Food Safety & Modernization Act'
Comments (3)Scott, Bill 5-10 is the Food Safety and Modernization Act of 2010, not 2009. It should be fairly obvious that the FDA intends to continue pushing more regulatory laws on the public as well as small farmers. Do we need this one? Not in my opinion. Legislators introduce bills such as this under the guise of "food safety" which the FDA will enforce if passed. Then the FDA will hypocritically at the same time not allow labeling of GMO foods, as well as ALLOWING overarching power to Monsanto to continue their mafia style control of GMO seeds, etc, etc, adnauseum. I for one am for less legislation over what small growers can produce, market and what consumers like myself can and can't buy, eat, or know what the heck is in it. In fact, I'm also opposed to the continual cramming of more and more legislation down the public's throat, PERIOD! It seems like the more laws being passed, the less freedom we have, not more. Anyway, this link below lists some of Senator Tom Coburn's objections to Bill 5-10 which are not without merit. One of which is the EXPENSE of enforcing it, if passed. I'm sure most tax payers would agree they are already being taxed to death on nearly every front. Here is a link that might be useful: Sen Coburn Opposes Bill 5-10 of 2010...See MoreEvil S510 Food 'Safety Act' passes Senate
Comments (23)I haven't commented yet and had tried to stay away from it as I try to avoid politics and policies on garden forums. Also till recently I hadn't studied it a lot. I did know most of the farmers here were against it. I have some concerns. Not about what will happen immediately but in the future. One of my concerns is why Monsanto and a few others lobbied so hard for it and also spent a fair amount in support of some legislators. I don't feel it will impact the small garden grower saving seeds for a long time if ever. Another concern is it may in time affect small seed vendors. I remember when Cargill and a few others got laws passed that eventually forced many of the small locker plants out of business. I was good friends and did business with several of them and know what happened. The initial law didn't do it but allowed the means to gradually tighten the screw till many were forced out. I can remember in the 70's when there were 8 locker plants within 60 miles. For the last 10 years there has been 2. Now with the increase in demand of people wanting either to fatten their own or buy meat they know how it was raised and also some easing of a few regulations there has been another open up. The goal of any corporation is too obtain a bigger share of the market. Whether that be a packing plant or a seed business. One way to eliminate competition is by legislation. And one way to get laws passed is too say it is for food safety. I have emailed one of my legislators asking questions. Other than that not a lot I can do but keep informed and watch how it plays out. Personally I try not to get too worked up over things I have no control of. Jay...See MoreImportant Message From Food Lion Stores
Comments (7)This whole thing has me scratching my head. There's been some peanut farms with trouble and one major company with problems. It's almost like there's a surprise when a company that uses a, how to describe it... low quality supplier? for their supplies has to recall products. I was talking to a lady at the store the other day and I commented how well stocked the peanut butter shelves were. I like Skippy and it was on sale for $1.49/jar. She and I agreed on this. I had two jars in my cart and she was getting some. We agreed that there was no need to fear the major brands. Just avoid the peanut butter added items where the companies don't do quality control on the product themselves. As I said, I bought two jars. They'll be on the shelf for a while anyway just in case. But the places that use it as an additive and don't care who the supplier is, to me would be suspect. At this point though, I would not buy a store brand or generic brand of jar peanut butter. Probably safe? Yeah. Worth the risk? Not to me. I found it curious that Target pulled a bunch of items (in their house brand) to be on the safe side. I commend them for being proactive. But then I noticed a number of other items they had on the shelf containing peanuts that they didn't pull. Again, I'm not running in fear, but I found it curious....See MoreFDA launches tougher oversight of supplements
Comments (13)I copied and pasted for those not able to get in. FDA launches tougher oversight of supplements Agency plans to overhaul 25-year-old rules to protect consumers and spur innovation. By Laurie McGinley February 11 at 11:02 AM The Food and Drug Administration said Monday it plans to beef up oversight of the sprawling, $50-billion-a-year dietary supplements industry, warning that the sector’s explosive growth has resulted in risks to consumers — such as an increase in supplements “spiked” with unlisted drug ingredients, and false and misleading claims about health benefits. The agency underscored the need for greater oversight by announcing it had sent 12 warning letters and five advisory letters earlier this month to companies the FDA said are selling dozens of products that contain unapproved drugs or make illegal claims for treating Alzheimer’s and other serious diseases. FDA Commissioner Scott Gottlieb saidthe agency is planning policy changes that could lead to the most important regulatory modernization since enactment of the 1994 Dietary Supplement Health and Education Act, which considers supplements safe until proved otherwise. Gottlieb said in an interview that while most supplement makers are responsible, the huge growth in the industry has allowed “bad actors” to sell dangerous products or ones that carry unproven claims. “I’m concerned that changes in the supplement market may have outpaced the evolution of our own policies and our capacity to manage emerging risks,” he said. Under the 1994 law, dietary supplements are regulated as food and, therefore, are not subject to premarket approval or the kind of safety and effectiveness testing required for drugs. Since the law was enacted, the industry has grown from 4,000 products and $4 billion a year in sales to as many as 80,000 products and $50 billion in sales, according to the FDA. While the FDA doesn’t clear the products ahead of time, it is charged with removing unsafe ones from the market. Three out of four Americans take a dietary supplement on a regular basis, and for older Americans, the proportion is four out of five, the agency said. One in three children also take supplements. Gottlieb said he plans a “balanced approach” to improve safety, reduce inaccurate claims and encourage industry innovation. For example, the agency plans to create a rapid-response tool to quickly alert the public if a supplement contains an illegal and potentially dangerous ingredient. It intends to streamline the handling of supplements containing prescription drugs such as the generic version of Viagra and to increase enforcement actions. In a nod to the industry, he said the agency would review its regulations on new dietary ingredients to make sure they are flexible enough to ensure product improvements. And he promised to call a public meeting to discuss that and other topics. Gottlieb also waded into an intense debate over whether there should be a mandatory FDA registry where supplement makers would be required to list their products and ingredients. He said mandatory listing “could provide significant benefits by improving transparency in the marketplace” and allowing the FDA to focus its enforcement efforts. But he acknowledged that such a major change likely would require legislation. Manufacturers are supposed to register their facilities with the FDA — but are not required to list their products or ingredients. It’s not clear how many are complying with the minimal requirement. The result is that the agency doesn’t have a clear idea of who is making what. Sandra Eskin, who directs the food safety project at Pew Trusts, welcomed Gottlieb’s comments and stressed the need for mandatory listing. “FDA needs to know what supplement products each company makes, as well as the ingredients and copies of the product labels,” she said. “This information is the cornerstone of an effective oversight and enforcement system, and Congress should require that supplement companies provide it to the agency.” Steve Mister, president and chief executive of the Council for Responsible Nutrition, which represents supplement makers, said in a statement that the FDA “shares our vision to further develop the thriving, innovative and safe marketplace for dietary supplements.” Increasingly, officials and public health experts have become concerned about unsafe ingredients — such as the active ingredients in drugs, often from overseas — showing up in supplements. An analysis published in October, written by a team from the California Department of Public Health, found unapproved and sometimes dangerous drugs in 746 dietary supplements, almost all of them marketed for sexual enhancement, weight loss or muscle growth. The drugs included sildenafil — the active ingredient in Viagra — and steroids in muscle-building products. In the fall, the FDA warned consumers to avoid Rhino male enhancement products that contained sildenafil. It said it had received reports of people experiencing chest pain, severe headaches and prolonged erections after taking a Rhino product. The agency also warned companies marketing supplements for opioid addiction that contained an unapproved antidepressant called tianeptine. Dietary supplement makers are allowed to make what are called “structure/function claims” on how a nutrient or dietary ingredient affects the body — for example, “calcium builds strong bones.” But they aren’t permitted to say their products treat or cure specific diseases such as osteoporosis. Such claims would mean the product would be regulated as a drug and subject to premarket approval requirements....See More- 4 years ago
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