The U.S. Food and Drug Administration has warned Erickson Dairy of Neillsville, WI, that it was found to be in violation of the Federal Food, Drug and Cosmetic Act after inspections at the dairy operation conducted on Dec. 2, 4, and 6, 2013. On March 3, 2014, FDA’s Minneapolis District Office wrote to the dairy to inform the owners and that the agency was citing Erickson Dairy for selling a cow for slaughter that was considered adulterated because of unacceptable levels of drug residues in the cow’s tissues. The investigation also found that the dairy had adulterated three new animal drugs by not using them as directed by their approved labeling or on the lawful order of a licensed veterinarian. The letter directed Erikson Dairy to “take prompt action to correct” the cited problems and to “establish procedures to ensure that these violations do not recur.” FDA requires a written response detailing steps for such compliance from all recipients of warning letters within 15 days of receipt of the letter.
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