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Establish Current Good Manufacturing Practice and Hazard Analysis and Risk-Based Preventive Controls for Food for AnimalsThe FDA Food Safety Modernization Act (FSMA) Preventive Controls for Animal Food rule is now final, and compliance dates for some businesses begin in September 2016.This final rule is the product of an unprecedented level of outreach by the FDA to industry, consumer groups, the agency’s federal, state, local and tribal regulatory counterparts, academia and other stakeholders. …

What is Ultra Safe Technology(UST)?Ultra Safe Technology is a revolutionary new line of brooms and brushes that help improve food safety and quality,minimize food waste and increase cleaning efficiency. These new products from Vikan comply with food safetyregulations and minimize the risk of contamination hazards. The innovative technology utilizesenhanced bristle security units directly molded to the brush block, removing any gaps or seams while offeringunprecedented br …

FDA Consumer Advice on Shree Baidyanath Brand Ayurvedic Dietary Supplements 09/17/2015 FDA Consumer Advice on Shree Baidyanath Brand Ayurvedic Dietary Supplements September 17, 2015 What you need to know Consumers who have used any of the Baidyanath brand Ayurvedic dietary supplements listed below should stop using them and consult their health care provider. Testing by the New York Department of Health and the U.S. Food and Drug Administration has …

Karoun Dairies, Inc. Issues Nationwide Voluntary Recall of Various Cheeses Because of Possible Health RiskContact: Consumer: 866-272-9393 Media: 866-272-9376FOR IMMEDIATE RELEASE — September 16, 2015 — San Fernando, CA — Today Karoun Dairies, Inc. announced that it is voluntarily recalling a variety of cheeses it distributes due to possible contamination with Listeria monocytogenes. To date, no product has tested positive for Listeria but in view of the association with listeriosis cases Karoun …

Recalls are actions taken by a firm to remove a product from the market. Recalls may be conducted on a firm's own initiative, by FDA request, or by FDA order under statutory authority.Class I recall: a situation in which there is a reasonable probability that the use of or exposure to a violative product will cause serious adverse health consequences or death. Class II recall: a situation in which use of or exposure to a violative product may cause temporary or medically reversible adverse heal …