Aurobindo Pharma USA, Inc. Initiates Voluntary Nationwide Consumer Level Recall of 80 Lots of Amlodipine Valsartan Tablets USP, Valsartan HCTZ Tablets, USP and Valsartan Tablets USP, Due to the Detection of NDEA (N-Nitrosodiethylamine) Impurity - FDA Safety Alerts & Drug Recalls

Aurobindo Pharma USA, Inc. is conducting a voluntary recall of 80 lots of Amlodipine Valsartan Tablets USP, Valsartan HCTZ Tablets, USP and Valsartan Tablets USP to the consumer level due to the detection of trace amounts of an unexpected impurity found in the finished drug product. The impurity detected in the finished drug product is N-nitrosodiethylamine (NDEA), which is a substance that occurs naturally in certain foods, drinking water, air pollution, and industrial processes, and has been classified as a probable human carcinogen as per International Agency for Research on Cancer (IARC) classification. To date, Aurobindo Pharma USA, Inc. has not received any reports of adverse events related to this recall.

from Food and Drug Administration--Recalls/Safety Alerts http://bit.ly/2F0y5vT
via IFTTT

Apio Inc. Expands Voluntary Recall of Eat Smart Salad Shake Ups Single-Serve Bowls - FDA Safety Alerts & Drug Recalls

Apio Inc. of Guadalupe, California is expanding a voluntary recall of Eat Smart Salad Shake Ups single-serve bowls. The recall comes after the Canadian Food Inspection Agency (CFIA) informed the company that another random sample of Eat Smart Salad Shake Ups Sweet Kale/Chou Frise Doux 156 gr. single-serve bowls (5.5oz) with Best Before Date of Dec 29, 2018, Lot 112 346, tested positive for Listeria monocytogenes, an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems.

from Food and Drug Administration--Recalls/Safety Alerts http://bit.ly/2Smqmwe
via IFTTT

Columbia River Natural Pet Foods Inc. Voluntarily Expands Recall to Include Cow Pie and Chicken & Vegetables Fresh Frozen Meats for Dogs and Cats Due to Possible Health Risk - FDA Safety Alerts & Drug Recalls

Columbia River Natural Pet Foods of Vancouver, WA is voluntarily expanding their current recall to include additional products: 261 packages of Cow Pie Lot # 72618 and 82 packages of Chicken & Vegetables Lot# 111518 fresh frozen meats for dogs and cats, produced in July 2018 and November 2018, due to their potential to be contaminated with Salmonella and Listeria monocytogenes

from Food and Drug Administration--Recalls/Safety Alerts http://bit.ly/2RkBE72
via IFTTT

Funky Chunky, Llc Issues Allergy Alert on Undeclared Almond and Cashew Tree-Nut in 10 Oz. Nutty Choco Pop Found in Chocolate Popcorn Gift Box, Holiday Crowd Pleaser and Crowd Pleaser Gifts - FDA Safety Alerts & Drug Recalls

Funky Chunky, LLC of Eden Prairie, MN is recalling 10 oz Nutty Choco Pop Gift Box, 50 oz. Holiday Crowd Pleaser and 50 oz. Crowd Pleaser, because it may contain undeclared Almond and Cashew Tree Nut. People who have an allergy or severe sensitivity to Almonds and Cashews run the risk of serious or life-threatening allergic reaction if they consume these products.

from Food and Drug Administration--Recalls/Safety Alerts http://bit.ly/2V2gut9
via IFTTT

FDA permits marketing of a diagnostic test to aid in measuring nutrients in breast milk - FDA Press Releases

The FDA authorized use of a new test that measures nutrients in breast milk providing healthcare professionals with tool to aid in the nutritional management of newborns.

from Food and Drug Administration--Press Releases http://bit.ly/2ELGYdA
via IFTTT

FDA approves new treatment for adult patients with rare, life-threatening blood disease - FDA Press Releases

The FDA approved Ultomiris (ravulizumab) injection for the treatment of adult patients with paroxysmal nocturnal hemoglobinuria (PNH), a rare and life-threatening blood disease.

from Food and Drug Administration--Press Releases http://bit.ly/2SYb2FY
via IFTTT

FDA approves first treatment for rare blood disease - FDA Press Releases

The FDA approved Elzonris (tagraxofusp-erzs) infusion for the treatment of blastic plasmacytoid dendritic cell neoplasm (BPDCN) in adults and in pediatric patients, two years of age and older.

from Food and Drug Administration--Press Releases http://bit.ly/2UZUDm8
via IFTTT

Inspired Organics Issues Voluntary Recall of Organic Nut & Seed Butters Due to Potential Health Risk - FDA Safety Alerts & Drug Recalls

Inspired Organics, LLC has issued a voluntary recall of Organic Almond, Peanut, and Tahini Butters due to potential contamination of Listeria monocytogenes. Listeria monocytogenes is an organism, which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems. Although healthy individuals may suffer only short- term symptoms such as high fever, severe headache, stiffness, nausea, abdominal pain and diarrhea, Listeria infection can cause miscarriages and stillbirths among pregnant women.

from Food and Drug Administration--Recalls/Safety Alerts https://ift.tt/2SjbDSR
via IFTTT

Statement from FDA Commissioner Scott Gottlieb, M.D., on signing of the Agriculture Improvement Act and the agency’s regulation of products containing cannabis and cannabis-derived compounds - FDA Press Releases

Statement from FDA Commissioner Scott Gottlieb, M.D., on signing of the Agriculture Improvement Act and the agency’s regulation of products containing cannabis and cannabis-derived compounds

from Food and Drug Administration--Press Releases https://ift.tt/2QHHWOh
via IFTTT

Terrific Care, LLC. / Medex Supply Dist, Inc. issues Nationwide Recall of CoaguChek Test Strips - FDA Safety Alerts & Drug Recalls

On 12/19/2018, Terrific Care, LLC. / Medex Supply Dist, Inc. initiated a nationwide recall of Roche CoaguChek test strips distributed directly to U.S. consumers by Terrific Care, LLC. / Medex Supply Dist, Inc. The products have been found to inaccurately report high INR test results.

from Food and Drug Administration--Recalls/Safety Alerts https://ift.tt/2SbSIsP
via IFTTT

Torrent Pharmaceuticals Limited Issues Voluntary Nationwide Recall of Losartan Potassium Tablets, USP - FDA Safety Alerts & Drug Recalls

Torrent Pharmaceuticals Limited is voluntarily recalling 2 lots of Losartan potassium tablets, USP to the consumer level due to the detection of trace amounts of an unexpected impurity found in an active pharmaceutical ingredient (API) manufactured by Hetero Labs Limited. The impurity detected in the API is N-nitrosodiethylamine (NDEA), which is a substance that occurs naturally in certain foods, drinking water, air pollution, and industrial processes, and has been classified as a probable human carcinogen as per International Agency for Research on Cancer (IARC) classification.

from Food and Drug Administration--Recalls/Safety Alerts https://ift.tt/2ExYj90
via IFTTT

Statement from FDA Commissioner Scott Gottlieb, M.D., on new steps to strengthen the long-term safety oversight of the Essure device following discontinuation of its U.S. sales - FDA Press Releases

The FDA provides update on Essure postmarket review study as company prepares to halt sales of the device on December 31.

from Food and Drug Administration--Press Releases https://ift.tt/2LsjxX5
via IFTTT

FDA warns about safety risks of teething necklaces, bracelets to relieve teething pain or to provide sensory stimulation - FDA Press Releases

FDA alerted parents, caregivers and health care providers to the safety risks that jewelry used for relieving teething pain pose for children.

from Food and Drug Administration--Press Releases https://ift.tt/2PPdtIU
via IFTTT

FDA sends warning to company for marketing dangerous unapproved stem cell products that put patients at risk and puts other stem cell firms, providers on notice - FDA Press Releases

FDA sends warning letter to Genetech, Inc. and letters to other companies to reiterate the FDA’s compliance and enforcement policy regarding stem cells.

from Food and Drug Administration--Press Releases https://ift.tt/2ECqmEY
via IFTTT

Wegmans Issues Voluntary Recall of Fresh Cauliflower Rice, Veggie/Cauliflower Rice Blend and Stir-Fry Mix with Cauliflower - FDA Safety Alerts & Drug Recalls

Rochester, NY – Wegmans Food Markets, Inc. has issued a voluntary recall of fresh Cauliflower Rice, Veggie Cauliflower Rice Blend and Stir-Fry Mix with Cauliflower, sold in the produce department between 12/7/18 and 12/18/18, because it may be contaminated with Escherichia coli O157:H7 bacteria (E. Coli O157:H7). E. coli O157:H7 causes a diarrheal illness often with bloody stools. Although most healthy adults can recover completely within a week, some people can develop a form of kidney failure called Hemolytic Uremic Syndrome (HUS). HUS is most likely to occur in young children and the elderly. The condition can lead to serious kidney damage and even death.

from Food and Drug Administration--Recalls/Safety Alerts https://ift.tt/2Gwwz7r
via IFTTT

Medtronic Announces Worldwide Voluntary Field Corrective Action; Company Issues Software Update for Puritan Bennett™ 980 (Pb980) Ventilator Series - FDA Safety Alerts & Drug Recalls

Medtronic (NYSE:MDT) is notifying customers worldwide of a voluntary field corrective action for its Puritan Bennett™ 980 (PB980) ventilator series. Medtronic initiated this field action on September 19, 2018.

from Food and Drug Administration--Recalls/Safety Alerts https://ift.tt/2CnHr3d
via IFTTT

Statement from FDA Commissioner Scott Gottlieb, M.D., and Jeff Shuren, M.D., Director of the Center for Devices and Radiological Health, on new steps to promote innovations in medical devices that help advance patient safety - FDA Press Releases

FDA announces steps being taken on two medical device programs: finalizing guidance on the Breakthrough Device Program and announcing plans for a new Safer Technologies Program (STeP).

from Food and Drug Administration--Press Releases https://ift.tt/2UUExKH
via IFTTT

Statement from FDA Commissioner Scott Gottlieb, M.D. on the FDA’s 2017 report on declining sales/distribution of antimicrobial drugs for food animals, a reflection of improved antimicrobial stewardship - FDA Press Releases

FDA’s 2017 report of sales/distribution data for antimicrobial drugs for food animals showed a continued decline in sales, a reflection of improved antimicrobial stewardship

from Food and Drug Administration--Press Releases https://ift.tt/2Bq9PjE
via IFTTT

Two novel quinomycins discovered by UPLC-MS from Stretomyces sp. HCCB11876 - Journal of Antibiotics

Two novel quinomycins discovered by UPLC-MS from Stretomyces sp. HCCB11876

Two novel quinomycins discovered by UPLC-MS from Stretomyces sp. HCCB11876, Published online: 18 December 2018; doi:10.1038/s41429-018-0132-1

Two novel quinomycins discovered by UPLC-MS from Stretomyces sp. HCCB11876

from The Journal of Antibiotics - Issue - nature.com science feeds https://ift.tt/2EBHUBm
via IFTTT

Adam Bros. Farming, Inc. Recalls Red and Green Leaf Lettuce and Cauliflower Because of Possible Health Risk - FDA Safety Alerts & Drug Recalls

Adam Bros. Farming, Inc. of Santa Maria, California is recalling red leaf lettuce, green leaf lettuce and cauliflower harvested on November 27 through 30, 2018 out of an abundance of caution, because it may be contaminated with Escherichia coli O157:H7 bacteria (E. Coli O157:H7).

from Food and Drug Administration--Recalls/Safety Alerts https://ift.tt/2PHfpmB
via IFTTT

Atherstone Foods Inc Issues Allergy Alert on Undeclared Soy in “Greens and Grains Hummus and Quinoa Tabouleh Wrap” - FDA Safety Alerts & Drug Recalls

ATHERSTONE FOODS INC of Richmond, CA is recalling 14.6 ounce (414g) Greens and Grains Hummus and Quinoa Tabouleh Wrap, because it may contain undeclared soy, people who have an allergy or severe sensitivity to soy run the risk of serious or life-threatening allergic reaction if they consume these products.

from Food and Drug Administration--Recalls/Safety Alerts https://ift.tt/2S1CLp4
via IFTTT

Enovachem Pharmaceuticals Issues Voluntary Nationwide Recall of Dyural-40 and Dyural-80 Convenience Kits Containing Recalled Sodium Chloride Injection, USP, 0.9% Due to Latex Hazard - FDA Safety Alerts & Drug Recalls

Torrance, CA, Asclemed USA Inc is voluntarily recalling 20 lots of Dyural-40 and 61 lots of Dyural-80, to the user level. The products include recalled Sodium Chloride, USP, 0.9% manufactured by Fresenius Kabi, which has been recalled due to product labeling incorrectly stating stoppers do not contain latex.

from Food and Drug Administration--Recalls/Safety Alerts https://ift.tt/2Ln0NIC
via IFTTT

Michigan-based food manufacturer agrees to stop operations after repeated food safety violations - FDA Press Releases

Saranac Brand Foods, Inc. specialized in a variety of 35 different ready-to-eat foods, including prepared salads, dips, and sauces.

from Food and Drug Administration--Press Releases https://ift.tt/2zZlAgU
via IFTTT

Inspired Organics Issues Voluntary Recall of Organic Almond Butter Due to Potential Health Risk - FDA Safety Alerts & Drug Recalls

Inspired Organics, LLC has issued a voluntary recall of Organic Almond Butter due to potential contamination of Listeria monocytogenes. Listeria monocytogenes is an organism, which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems. Although healthy individuals may suffer only short-term symptoms such as high fever, severe headache, stiffness, nausea, abdominal pain and diarrhea, Listeria infection can cause miscarriages and stillbirths among pregnant women.

from Food and Drug Administration--Recalls/Safety Alerts https://ift.tt/2SSbqWn
via IFTTT

Semisynthesis and antibacterial activities of nidulin derivatives - Journal of Antibiotics

Semisynthesis and antibacterial activities of nidulin derivatives

Semisynthesis and antibacterial activities of nidulin derivatives, Published online: 17 December 2018; doi:10.1038/s41429-018-0133-0

Semisynthesis and antibacterial activities of nidulin derivatives

from The Journal of Antibiotics - Issue - nature.com science feeds https://ift.tt/2S69yt4
via IFTTT

Spokane Produce Voluntarily Recalls Northwest Cuisine Creations and Fresh&Local Sandwiches and Green Leaf Lettuce Filets - FDA Safety Alerts & Drug Recalls

Spokane Produce Inc. of Spokane, WA initiates a voluntary recall of sandwiches containing green leaf lettuce and foodservice lettuce filets following notice of a produce industry ingredient recall by Adam Bros. Farming Inc. Sandwich products bearing the Northwest Cuisine Creations and Fresh&Local labels. These prod- ucts are recalled because they may be contaminated with Escherichia coli O157:H7 bacteria (E. Coli O157:H7). E. coli O157:H7 causes a diarrheal illness often with bloody stools. Although most healthy adults can recover completely within a week, some people can develop a form of kidney failure called Hemolytic Uremic Syndrome (HUS). HUS is most likely to occur in young children and the elderly. The condition can lead to serious kidney damage and even death

from Food and Drug Administration--Recalls/Safety Alerts https://ift.tt/2ChCoS5
via IFTTT

Apio, Inc. Voluntarily Recalls Five Skus of Eat Smart Single-Serve Salad Shake Ups™ - FDA Safety Alerts & Drug Recalls

Apio, Inc. of Guadalupe, California is voluntarily recalling five SKUs of Eat Smart® Single-Serve Salad Shake Ups™ (bowls). The recall comes after the Canadian Food Inspection Agency (CFIA) informed the company that one random sample of Eat Smart Single-Serve Salad Shake Ups Sweet Kale/Chou Frise Doux 156 gr. (5.5oz) with Best Before of Dec 14, 2018 tested positive for Listeria Monocytogenes. As a precautionary measure, we are recalling all products produced on the same day, same production line, as the one sample that tested positive by CFIA. At this time, we are not aware of any illnesses linked by health officials to this recall and no other products are affected by this recall.

from Food and Drug Administration--Recalls/Safety Alerts https://ift.tt/2Bna0vU
via IFTTT

Statement from FDA Commissioner Scott Gottlieb, M.D. and FDA Deputy Commissioner Frank Yiannas on new findings and updated consumer recommendations related to the romaine lettuce E. coli O157:H7 outbreak investigation - FDA Press Releases

Statement from FDA Commissioner Scott Gottlieb, M.D. and FDA Deputy Commissioner Frank Yiannas on new findings and updated consumer recommendations related to the romaine lettuce E. coli O157:H7 outbreak investigation

from Food and Drug Administration--Press Releases https://ift.tt/2S0cMhY
via IFTTT

Statement from FDA Commissioner Scott Gottlieb, M.D. and Director of FDA’s Center for Drug Evaluation and Research Janet Woodcock, M.D., on efforts to modernize generic drug labels while maintaining the efficiency of generic development - FDA Press Releases

FDA announces withdrawal of the proposed rule, Supplemental Applications Proposing Labeling Changes for Approved Drugs and Biological Products

from Food and Drug Administration--Press Releases https://ift.tt/2C9HVtz
via IFTTT

Del Monte Foods Announces Limited Recall of Canned Fiesta Corn Seasoned with Red & Green Peppers Due to Under Processing - FDA Safety Alerts & Drug Recalls

Del Monte Foods Inc. announced a recall of 64,242 cases of FIESTA CORN Seasoned with Red & Green Peppers due to under-processing. These deviations were part of the commercial sterilization process and could result in contamination by spoilage organisms or pathogens, which could lead to life-threatening illness if consumed. It is important to note that there have been no reports of illness associated with these products to date. No other production codes or products are affected by this recall.

from Food and Drug Administration--Recalls/Safety Alerts https://ift.tt/2Le2vw3
via IFTTT

Kimberly-Clark Announces Voluntary Recall of U by Kotex® Sleek® Tampons, Regular Absorbency,Throughout U.S. and Canada - FDA Safety Alerts & Drug Recalls

Kimberly-Clark announced a voluntary product recall of its U by Kotex® Sleek® Tampons, Regular Absorbency, sold throughout the United States and Canada for a quality-related defect that could impact the performance of this product.

from Food and Drug Administration--Recalls/Safety Alerts https://ift.tt/2ErW2gn
via IFTTT

Statement from FDA Commissioner Scott Gottlieb, M.D., on the agency’s efforts to improve drug quality through vigilant oversight of data integrity and good manufacturing practice - FDA Press Releases

FDA releases guidance with recommendations for drug manufacturers regarding good manufacturing practices and data integrity

from Food and Drug Administration--Press Releases https://ift.tt/2ROtOzu
via IFTTT

Mannonerolidol, a new nerolidol mannoside from culture broth of Schizophyllum commune - Journal of Antibiotics

Mannonerolidol, a new nerolidol mannoside from culture broth of Schizophyllum commune

Mannonerolidol, a new nerolidol mannoside from culture broth of <i>Schizophyllum commune</i>, Published online: 12 December 2018; doi:10.1038/s41429-018-0130-3

Mannonerolidol, a new nerolidol mannoside from culture broth of Schizophyllum commune

from The Journal of Antibiotics - Issue - nature.com science feeds https://ift.tt/2BdgAVJ
via IFTTT

Bioactive secondary metabolites from an endophytic fungus Phoma sp. PF2 derived from Artemisia princeps Pamp. - Journal of Antibiotics

Bioactive secondary metabolites from an endophytic fungus Phoma sp. PF2 derived from Artemisia princeps Pamp.

Bioactive secondary metabolites from an endophytic fungus <i>Phoma</i> sp. PF2 derived from <i>Artemisia princeps</i> Pamp., Published online: 12 December 2018; doi:10.1038/s41429-018-0131-2

Bioactive secondary metabolites from an endophytic fungus Phoma sp. PF2 derived from Artemisia princeps Pamp.

from The Journal of Antibiotics - Issue - nature.com science feeds https://ift.tt/2Bb7Hfy
via IFTTT

Moonstruck Chocolate Co. Issues Allergy Alert On Undeclared Hazelnuts In 4 Oz. Sea Salt Caramels Tumbled In Milk Chocolate - FDA Safety Alerts & Drug Recalls

Moonstruck Chocolate Company of Portland, Oregon is recalling 600/4 oz. bags of Sea Salt Caramels Tumbled In Milk Chocolate, because it may contain undeclared hazelnuts. People who have an allergy or severe sensitivity to hazelnuts run the risk of a serious or life-threatening allergic reaction if they consume this product.

from Food and Drug Administration--Recalls/Safety Alerts https://ift.tt/2QwbzCo
via IFTTT

FDA warns API manufacturer involved in valsartan recall, provides information for patients taking these medications - FDA Press Releases

FDA update on the ongoing investigation into angiotensin II receptor blocker impurities, recalls and current findings.

from Food and Drug Administration--Press Releases https://ift.tt/2GdPmnI
via IFTTT

Inspired Organics Issues Voluntary Recall of Organic Sunflower Butter Due to Potential Health Risk - FDA Safety Alerts & Drug Recalls

Inspired Organics, LLC has issued a voluntary recall of Organic Sunflower Butter due to potential contamination of Listeria monocytogenes. Listeria monocytogenes is an organism, which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems. Although healthy individuals may suffer only short-term symptoms such as high fever, severe headache, stiffness, nausea, abdominal pain and diarrhea, Listeria infection can cause miscarriages and stillbirths among pregnant women.

from Food and Drug Administration--Recalls/Safety Alerts https://ift.tt/2zWFE3t
via IFTTT

Statement from FDA Commissioner Scott Gottlieb, M.D., on new actions advancing the agency’s biosimilars policy framework - FDA Press Releases

FDA announces new actions advancing the agency’s biosimilars policy framework

from Food and Drug Administration--Press Releases https://ift.tt/2PvU7IM
via IFTTT

Statement from Jeff Shuren, M.D., J.D., Director of the Center for Devices and Radiological Health, on updated safety communication about rates of duodenoscope contamination from preliminary postmarket data - FDA Press Releases

FDA provides updates to postmarketing studies that agency ordered three manufacturers of duodenoscopes to conduct to assess bacterial contamination of devices.

from Food and Drug Administration--Press Releases https://ift.tt/2rwXPIA
via IFTTT

FDA clears mobile medical app to help those with opioid use disorder stay in recovery programs - FDA Press Releases

FDA clears a mobile medical application (app) to help increase retention (the amount of time a patient participates) in an outpatient treatment program for individuals with opioid use disorder

from Food and Drug Administration--Press Releases https://ift.tt/2QJTYWG
via IFTTT

The J.M. Smucker Company Issues Voluntary Recall of Specific Lots of - FDA Safety Alerts & Drug Recalls

The J.M. Smucker Company today announced a voluntary recall of specific lots of 9Lives® Protein Plus® wet, canned cat food due to possible low levels of thiamine (Vitamin B1). No illnesses related to this issue have been reported to date and the product is being recalled out of an abundance of caution.

from Food and Drug Administration--Recalls/Safety Alerts https://ift.tt/2rrK8KQ
via IFTTT

New tetrahydroquinoline and indoline compounds containing a hydroxy cyclopentenone, virantmycin B and C, produced by Streptomyces sp. AM-2504 - Journal of Antibiotics

New tetrahydroquinoline and indoline compounds containing a hydroxy cyclopentenone, virantmycin B and C, produced by Streptomyces sp. AM-2504

New tetrahydroquinoline and indoline compounds containing a hydroxy cyclopentenone, virantmycin B and C, produced by <i>Streptomyces</i> sp. AM-2504, Published online: 10 December 2018; doi:10.1038/s41429-018-0117-0

New tetrahydroquinoline and indoline compounds containing a hydroxy cyclopentenone, virantmycin B and C, produced by Streptomyces sp. AM-2504

from The Journal of Antibiotics - Issue - nature.com science feeds https://ift.tt/2Eot6FP
via IFTTT

Statement from FDA Commissioner Scott Gottlieb, M.D. and Deputy Commissioner Anna Abram on new efforts to assure the quality of compounded drugs - FDA Press Releases

FDA releases guidance with recommendations for protecting patients from the risk of contaminated or substandard compounded products produced by outsourcing facilities.

from Food and Drug Administration--Press Releases https://ift.tt/2rt4Jyv
via IFTTT

Simpotentin, a new potentiator of amphotericin B activity against Candida albicans, produced by Simplicillium minatense FKI-4981 - Journal of Antibiotics

Simpotentin, a new potentiator of amphotericin B activity against Candida albicans, produced by Simplicillium minatense FKI-4981

Simpotentin, a new potentiator of amphotericin B activity against <i>Candida albicans</i>, produced by <i>Simplicillium minatense</i> FKI-4981, Published online: 10 December 2018; doi:10.1038/s41429-018-0128-x

Simpotentin, a new potentiator of amphotericin B activity against Candida albicans, produced by Simplicillium minatense FKI-4981

from The Journal of Antibiotics - Issue - nature.com science feeds https://ift.tt/2Qnds4e
via IFTTT

Fine Land Corp Issues Allergy Alert on Undeclared Milk Allergens in “Meiqili Durian Candy” - FDA Safety Alerts & Drug Recalls

Fine Land Corp is recalling it’s 12 ounce (340 g) Meiqili Durian Candy in plastic bag with clear window because it contains undeclared milk allergens. Consumers who are allergic to milk allergens may run the risk of serious or life – threatening allergic reactions if they consume this product.

from Food and Drug Administration--Recalls/Safety Alerts https://ift.tt/2Up5UfG
via IFTTT

Accra Super Market Issues Allergy Alert On Undeclared Peanuts In 'Suya Barbecue Seasoning' - FDA Safety Alerts & Drug Recalls

Accra Super Market of Worcester MA, is recalling 0.53 lbs packages of "Suya Barbecue Seasoning" because it may contain undeclared peanuts. People who have allergies to peanuts run the risk of serious or life-threatening allergic reaction if they consume this product.

from Food and Drug Administration--Recalls/Safety Alerts https://ift.tt/2BWa8US
via IFTTT

Kroger Louisville Division Recalls Abound Chicken and Brown Rice Dog Food Because of Elevated Vitamin D Levels - FDA Safety Alerts & Drug Recalls

Following a recall by Sunshine Mills, Inc., the Kroger Louisville division announced it has removed from sale Abound Chicken & Brown Rice Recipe dog food produced by the supplier. The dog food was sold in one Kroger store located at 2440 Bardstown Road in Louisville, KY. Only Abound Chicken & Brown Rice Recipe dog food with the listed UPC numbers and Best by Dates are affected by this recall. The recall was initiated because the product had the potential to contain an elevated level of Vitamin D, which may cause renal failure.

from Food and Drug Administration--Recalls/Safety Alerts https://ift.tt/2SAfyKH
via IFTTT

King Soopers and City Market Recalls Abound Chicken and Brown Rice Dog Food Because of Elevated Vitamin D Levels - FDA Safety Alerts & Drug Recalls

Following a recall by Sunshine Mills, Inc., King Soopers announced it has removed from sale Abound Chicken & Brown Rice Recipe dog food produced by Sunshine Mills, Inc. sold in King Soopers and City Market stores, located in Colorado, Utah, New Mexico and Wyoming. Only Abound Chicken & Brown Rice Recipe dog food with the listed UPC numbers and Best by Dates are affected by this recall. The recall was initiated because the product had the potential to contain an elevated level of Vitamin D, which may cause renal failure.

from Food and Drug Administration--Recalls/Safety Alerts https://ift.tt/2EirrS9
via IFTTT

Danone North America Issues Allergy Alert and Recall for Light & Fit Greek Crunch S’mores Flavor - FDA Safety Alerts & Drug Recalls

Danone North America is voluntarily recalling 3,521 cases of Light & Fit® Greek Crunch Nonfat Yogurt & Toppings S’Mores Flavor sold in the United States with an expiration date of December 30, 2018 and UPC of 36632 03825. It was discovered that some of the toppers sold on the product contain peanuts and are improperly labeled. People who have an allergy to peanuts run the risk of serious or life-threatening allergic reaction if they consume this product.

from Food and Drug Administration--Recalls/Safety Alerts https://ift.tt/2rquQG0
via IFTTT

Tris Pharma Issues Voluntary Nationwide Recall of Infants’ Ibuprofen Concentrated Oral Suspension, USP (NSAID) 50 mg per 1.25 mL, Due to Potential Higher Concentrations of Ibuprofen - FDA Safety Alerts & Drug Recalls

Tris Pharma, Inc. has voluntarily recalled three (3) lots of Infants’ Ibuprofen Concentrated Oral Suspension, USP (NSAID) 50 mg per 1.25 mL, to the retail level. The recalled lots of the product have been found to potentially have higher concentrations of ibuprofen.

from Food and Drug Administration--Recalls/Safety Alerts https://ift.tt/2QCDQWN
via IFTTT

Statement from FDA Commissioner Scott Gottlieb, M.D., on FDA’s new strategic framework to advance use of real-world evidence to support development of drugs and biologics - FDA Press Releases

FDA releases new strategic framework to advance use of real-world evidence to support development of drugs and biologics

from Food and Drug Administration--Press Releases https://ift.tt/2RJp5z6
via IFTTT

Statement from FDA Commissioner Scott Gottlieb, M.D., on the FDA’s new effort for developing and class labeling of in vitro companion diagnostics for classes of oncology therapeutic products - FDA Press Releases

Statement from FDA Commissioner Scott Gottlieb, M.D., on the FDA’s new effort for developing and class labeling of vitro companion diagnostics for classes of oncology therapeutic products

from Food and Drug Administration--Press Releases https://ift.tt/2UnRUm7
via IFTTT

Country Flavor Inc Issues Alert on Undeclared Sulfites In "Best Taste Brand Dried Bamboo Shoot" - FDA Safety Alerts & Drug Recalls

Country Favor Inc. of Maspeth, New York is recalling its 12 ounce packages of "Best Taste Brand DRIED BAMBOO SHOOT" food treats because they contained undeclared sulfites. Consumers who have severe sensitivity to sulfites run the risk of serious or life-threatening allergic reactions if they consume this product.

from Food and Drug Administration--Recalls/Safety Alerts https://ift.tt/2QhyGjR
via IFTTT

Columbia River Natural Pet Foods Inc. Recalls Cow Pie Fresh Frozen Meats for Dogs and Cats Because of Possible Listeria monocytogenes Health Risk - FDA Safety Alerts & Drug Recalls

Columbia River Natural Pet Foods of Vancouver, WA is voluntarily recalling 933 packages of Cow Pie fresh frozen meats for dogs and cats, produced in August 2017, because it has the potential to be contaminated with Listeria monocytogenes

from Food and Drug Administration--Recalls/Safety Alerts https://ift.tt/2RCishN
via IFTTT

Chukar Cherries Expands Recall of Ultra Dark Chocolate Product Due to Undeclared Milk - FDA Safety Alerts & Drug Recalls

Chukar Cherries of Prosser, WA expands a recall on Ultra Dark Chocolate product because it may contain undeclared milk. People who have an allergy or severe sensitivity to milk run the risk of serious or life-threatening allergic reaction if they consume these products.

from Food and Drug Administration--Recalls/Safety Alerts https://ift.tt/2zHpzPd
via IFTTT

Hiland Dairy Announces Voluntary Recall of Hiland Dairy Half-Gallon Whole Chocolate Milk - FDA Safety Alerts & Drug Recalls

Hiland Dairy is announcing a voluntary recall of half-gallon premium whole milk chocolate that is produced at the Kansas City, Missouri facility, over concerns the products may contain eggnog that could affect those individuals that have sensitivity to egg allergens. People who have an allergy or severe sensitivity to eggs run the risk of serious or life-threatening allergic reaction if they consume these products.

from Food and Drug Administration--Recalls/Safety Alerts https://ift.tt/2UfW0N1
via IFTTT

Mylan Expands Its Voluntary Nationwide Recall of Valsartan Tablets, USP, Amlodipine and Valsartan Tablets, USP, and Valsartan and Hydrochlorothiazide Tablets, USP, to all Lots Within Expiry Due to The Detection of Trace Amounts of NDEA (N-Nitrosodiethylamine) Impurity Found in the Active Pharmaceutical Ingredient - FDA Safety Alerts & Drug Recalls

– Mylan N.V. (NASDAQ: MYL) today announced that its U.S. based Mylan Pharmaceuticals business is expanding its consumer-level voluntary nationwide recall to include all lots of Valsartan-containing products within expiry. The 104 additional lots include 26 lots of Amlodipine and Valsartan Tablets, USP (including the 5mg/160mg, 10mg/160mg, 5mg/320mg and 10mg/320mg strengths), 51 lots of Valsartan Tablets, USP (including 40 mg, 80 mg, 160 mg and 320 mg strengths), and 27 lots of Valsartan and Hydrochlorothiazide Tablets, USP (80mg/12.5mg, 160mg/12.5mg, 160mg/25mg, 320mg/12.5mg and 320mg/25mg strengths).

from Food and Drug Administration--Recalls/Safety Alerts https://ift.tt/2riXmcC
via IFTTT

FDA takes new action to advance the development of reliable and beneficial genetic tests that can improve patient care - FDA Press Releases

FDA takes new action to advance the development of reliable and beneficial genetic tests that can improve patient care

from Food and Drug Administration--Press Releases https://ift.tt/2ARWxMe
via IFTTT

Isolation of ketomycin from Actinomycetes as an inhibitor of 2D and 3D cancer cell invasion - Journal of Antibiotics

Isolation of ketomycin from Actinomycetes as an inhibitor of 2D and 3D cancer cell invasion

Isolation of ketomycin from <i>Actinomycetes</i> as an inhibitor of 2D and 3D cancer cell invasion, Published online: 03 December 2018; doi:10.1038/s41429-018-0129-9

Isolation of ketomycin from Actinomycetes as an inhibitor of 2D and 3D cancer cell invasion

from The Journal of Antibiotics - Issue - nature.com science feeds https://ift.tt/2zG0QdS
via IFTTT