The Food and Drug Administration responded Monday to a four-year-old petition from the Center for Food Safety and the Institute for Agriculture and Trade Policy, stating that the agency was in the process of formally withdrawing approval for the use of arsenic-based drugs in animal feed. The letter states that sponsors of three of the four FDA-approved arsenic-containing compounds added to chicken, turkey and hog feed have withdrawn their products from the market and have requested that the FDA withdraw their approval. The agency is doing just that, but has denied the withdrawal of drugs associated with the fourth compound, choosing to pursue scientific research and evaluation. Of the 101 drug approvals for arsenic-based animal drugs, 98 will be withdrawn. First approved as animal feed additives in the 1940s, arsenic-containing compounds have been fed to poultry to induce weight gain. A 2006 IATP report estimated that more than 70 percent of all U.S. chickens raised for food were fed arsenic and tests of the chicken in our grocery stores indicated that half of it contained detectable arsenic. CFS and IATP’s 2009 petition called on FDA to withdraw its approval of the compounds, arguing that they are not necessary in animal feed and could pose a public health risk. Organic arsenic compounds, they argued, are not only toxic, but can also convert to cancer-causing inorganic arsenic inside of chickens, in manure-treated soil, and in humans. FDA’s response comes after CFS filed a lawsuit compelling the agency to do so.
The News Desk team at Food Safety News covers breaking developments, regulatory updates, recalls, and key topics shaping food safety today. These articles are produced collaboratively by our editorial staff.
A leading academic has warned that any plans for UK regulators to help industry grow could end up repeating past mistakes and impacting public health.
As part of modernization plans,
The FDA has issued final guidance for manufacturers of infant formula and laboratories conducting testing on infant formula.
The guidance was developed to help manufacturers and laboratories in the design,
As part of its enforcement activities, the Food and Drug Administration sends warning letters to entities under its jurisdiction. Some letters are not posted for public view until weeks or
The a2 Milk Company (“a2MC”) has recalled three specific batches of its imported a2 Platinum Premium USA label infant formula 0-12 months because of the presence of cereulide. The product
JXK Enterprises Inc. is recalling Boner Bears Chocolate, Lot #BB21125, after being notified that FDA laboratory analysis confirmed the presence of sildenafil, an active ingredient in the FDA-approved prescription drug
Total Nutrition Inc. of Deer Park, NY, is recalling TNVitamins Ultra Potent Complete Green Superfood and Doctor’s Pride Complete Green Superfood Ultra Potent Moringa Capsules because they have the
Bazzini LLC, of Allentown, PA, a co-manufacturer utilized by SkinnyDipped, is recalling a limited number of cases of SkinnyDipped Dark Chocolate Coconut Almond Bites, because of the possible presence of