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With some foodborne illness outbreaks traced to imported goods-gourmet cheese, for example-the Obama administration has strengthened its initiatives for improving food safety in the country, according to a Washington Post report.

The US Food and Drug Administration (FDA) has proposed a new policy intended to modernise and improve the quality of mammography, which is used for breast cancer screening and diagnosis.

The US Food and Drug Administration (FDA) has highlighted concerns about using robotically assisted surgical devices for mastectomies and other cancer surgeries, citing a lack of evidence for safety and effectiveness.

The US Food and Drug Administration (FDA) has labelled a recall of circular staplers by Johnson & Johnson (J&J) unit Ethicon as Class I, or high risk.

The US Food and Drug Administration (FDA) has sent warning letters to a Johnson & Johnson unit, Mentor Worldwide, and Sientra for failure to comply with its post-approval study requirements for breast implants.

Avanos Medical has secured US Food and Drug Administration (FDA) 501(k) clearance for its postoperative pain management device ON-Q Bolus.

The US Food and Drug Administration (FDA) has rejected Helius Medical Technologies' premarket submission for the Portable Neuromodulation Stimulator (PoNS) device due to a lack of data.

The US Food and Drug Administration (FDA) has granted clearance to Innoblative Designs' electrosurgical device SIRA RFA.

Compliance and enforcement actions by the US Food and Drug Administration (FDA) have dramatically declined under the Trump administration, with medical devices seeing the steepest drop, according to a new report.

The US Food and Drug Administration (FDA) has approved the new Cochlear Nucleus Profile Plus Series Cochlear Implant and the Nucleus 7 Sound Processor's new built-in connectivity.

Material sciences company W. L. Gore & Associates has received approval from the US Food and Drug Administration (FDA) for its Tag Conformable Thoracic Stent Graft, a thoracic endovascular aortic repair (TEVAR) device.

3D printing solutions provider Materialise has obtained clearance for its Mimics Enlight cardiovascular planning software suite from the US Food and Drug Administration (FDA).

Reports on Food Recalls says that it increase in 3rd quarter of 2013. Learn more about what affected that increase.

Tetra Pak Juice, nectar and still drinks are three categories of drinks with so many variants that all consumers, regardless of age, lifestyle and taste preferences, can find their favorites. Common to them all is that, to varying degrees, they contain the natural Mango juice or extract from fruit, vegetables or herbs. What the final product can be called is regulated by national and regional food legislation, but with some variation.​​ ​​​​​​​​​Mango Tetra Pak Juice - 100% fruit Juice Juice contains only the natural ingredients contained in fruit and vegetables, i.e. fruit juice or fruit juice concentrate, water, natural flavorings and fruit pulp. Whether the juice comes from concentrate or not, it undergoes a mild pasteurization​ process before packaging to ensure that the consumer gets a safe, high quality product, without any risk of unwanted micro-organisms. Product content and labeling of fruit juices are subject to different regulations that vary globally. In the USA there are standards set by the FDA and USDA, in the EU there are both mandatory directives and recommendations, and other regions may have a mixture of mandatory and voluntary standards.​ Nectar Within the beverage industry nectar is a fruit juice that is too thick to drink for example, from apricots, peaches and pears. The mango juice, or rather the puree, must therefore be diluted with water and have sugar added to make it drinkable. The fruit juice content in nectar can vary between 25 and 99 per cent.​ Still drinks The next step on the scale for less juice content is still drinks, namely fruit drinks with less than 25 per cent of fruit content. Some countries require that the juice content is stated on the package and others have a minimum requirement for juice content.

Omron Healthcare has launched a new FDA-approved blood pressure monitor, named Complete, with EKG capability.Developed in alliance with AliveCor, the new device features an upper arm cuff for simultaneous monitoring of blood pressure and EKG readings at home.

Know the relation between Food Safety and Hazard Analysis and Critical Control Points or what we all know as HACCP. Learn it only at Learn2serve Blog!