Hill’s Pet Nutrition Voluntarily Recalls Select Canned Dog Food for Excessive Vitamin D - FDA Safety Alerts & Drug Recalls

Hill’s Pet Nutrition is voluntarily recalling select canned dog food products due to potentially elevated levels of vitamin D. While vitamin D is an essential nutrient for dogs, ingestion of elevated levels can lead to potential health issues depending on the level of vitamin D and the length of exposure, and dogs may exhibit symptoms such as vomiting, loss of appetite, increased thirst, increased urination, excessive drooling, and weight loss. Vitamin D, when consumed at very high levels, can lead to serious health issues in dogs including renal dysfunction. Pet parents with dogs who have consumed any of the products listed and are exhibiting any of these signs should contact their veterinarian. In most cases, complete recovery is expected after discontinuation of feeding.

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

Statement from FDA Commissioner Scott Gottlieb, M.D., on 2019 efforts to advance the development of complex generics to improve patient access to medicines - FDA Press Releases

FDA Commissioner on 2019 efforts to advance the development of complex generics to improve patient access to medicines

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

FDA approves first generic Advair Diskus - FDA Press Releases

FDA approved the first generic of Advair Diskus for treatment of asthma and maintenance treatment of airflow obstruction and reducing exacerbations with COPD.

from Food and Drug Administration--Press Releases http://bit.ly/2Ghw5An
via IFTTT

Tris Pharma, Inc Expands Its Voluntary Nationwide Retail Recall of Ibuprofen Oral Suspension Drops, USP, 50 mg per 1.25 mL, Due to Higher Concentration of Ibuprofen - FDA Safety Alerts & Drug Recalls

Monmouth Junction, NJ, Tris Pharma, Inc. is expanding the scope of its November 2018 recall by adding three (3) additional lots of Ibuprofen Oral Suspension Drops, USP, 50 mg per 1.25 mL, to the retail (pharmacy) level. Some units from these batches have been found to have higher levels of Ibuprofen concentration.

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

Nature’s Rx Issues Voluntary Nationwide Recall of Silver Bullet 10x to Undeclared PDF-5 Inhibitors in the Product - FDA Safety Alerts & Drug Recalls

Nature’s Rx is voluntarily recalling quantity lots of Silver Bullet 10x, description of dosage form to the hospital, retail or consumer level. This recall has been initiated because the product was found to contain undeclared sildenafil and tadalafil, the active ingredient in Viagra and Cialis respectively, which are PDE-5 inhibitors. The undeclared PDE-5 inhibitors in the product may pose serious health risks because consumers with underlying medical issues may take the products without knowing that they can cause serious harm or interact in dangerous ways with other drugs they may be taking

from Food and Drug Administration--Recalls/Safety Alerts http://bit.ly/2Rr6WF9
via IFTTT

Statement from FDA Commissioner Scott Gottlieb, M.D., on the agency’s efforts to enhance the utility of the Orange Book to foster drug competition - FDA Press Releases

FDA announces new policies to ensure the Orange Book provides the greatest benefit to patients and providers, and generic drug developers.

from Food and Drug Administration--Press Releases http://bit.ly/2Gbo3ss
via IFTTT

Purina Animal Nutrition Voluntarily Recalling Purina® Honor® Show Chow® Showlamb Grower Due to Elevated Copper Level - FDA Safety Alerts & Drug Recalls

)– Purina Animal Nutrition is voluntarily recalling two lots of Purina® Honor® Show Chow® Showlamb Grower due to elevated copper levels. The feed is packaged in purple branded Purina Honor Show Chow bags.

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

Oskri Organics Corporation Recalls All Nut Butters because of Possible Health Risk - FDA Safety Alerts & Drug Recalls

Oskri Organics Corporation of Lake Mills, WI is recalling ALL Oskri Corporation manufactured nut butters. This recall has been initiated due to positive test results for Listeria monocytogenes found in multiple Oskri Corporation manufactured nut butters.

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

Two new glutarimide antibiotics from Streptomyces sp. HS-NF-780 - Journal of Antibiotics

Two new glutarimide antibiotics from Streptomyces sp. HS-NF-780

Two new glutarimide antibiotics from <i>Streptomyces</i> sp. HS-NF-780, Published online: 29 January 2019; doi:10.1038/s41429-019-0143-6

Two new glutarimide antibiotics from Streptomyces sp. HS-NF-780

from The Journal of Antibiotics - Issue - nature.com science feeds https://go.nature.com/2Bc8VYB
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 a record year for device innovation - FDA Press Releases

Review of 2018 device innovations, with record-setting 106 novel device approvals, and new actions FDA is taking to modernize approach to safety

from Food and Drug Administration--Press Releases http://bit.ly/2G5bWx3
via IFTTT

SL: Recall of Thrive Market Nut Butters Due to Potential Health Risk - FDA Safety Alerts & Drug Recalls

Thrive Market, Inc, is recalling all unexpired lots of the Thrive Market-branded nut butters listed below (“Product(s)”) due to the potential for contamination with Listeria monocytogenes. On January 21, 2019, one of our suppliers notified us that it was issuing a recall of all nut butters it has manufactured since January 2018 because of a positive test for Listeria monocytogenes in recent lots. Because the safety of our members is our absolute priority, we are expanding on our supplier’s recall and are voluntarily recalling all unexpired lots of all Thrive Market-branded nut butters manufactured by this supplier.

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

Mrs. Grissom’s Salads Issues a Voluntary Recall - FDA Safety Alerts & Drug Recalls

For immediate release- January 18,2019 – Nashville, TN – Mrs. Grissom’s Salads is voluntarily recalling a single days production of Mrs. Grissom’s SELECT Old Fashioned Pimento Cheese because of a labeling issue. Product produced on December 13, 2018 may have been packaged incorrectly, with the correct Pimento Cheese label on top lid, but a Chicken salad label on the container. The Pimento Cheese may contain allergens not listed on the products ingredient label, Specifically Milk.

from Food and Drug Administration--Recalls/Safety Alerts http://bit.ly/2TfUtG2
via IFTTT

Jac. Vandenberg, Inc. Recalls Fresh Peaches, Fresh Nectarines and Fresh Plums Because They May Be Contaminted with Listeria Monocytogenes - FDA Safety Alerts & Drug Recalls

Jac. Vandenberg, Inc. of Yonkers, New York is recalling 1,727 cartons of Fresh Peaches, 1,207 cartons of Fresh Nectarines and 365 cartons of Fresh Plums because they have the potential to be contaminated with 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/2FPoVno
via IFTTT

Statement from FDA Commissioner Scott Gottlieb, M.D., and Janet Woodcock, M.D., director of the Center for Drug Evaluation and Research on the FDA’s ongoing investigation into valsartan and ARB class impurities and the agency’s steps to address the root causes of the safety issues - FDA Press Releases

FDA describes the ongoing investigation into the ARB class impurities and agency’s steps to address the root causes of the safety issues

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

Satur Farms’ Recall of Baby Spinach Affects Prepared Food Items from Whole Foods Market Stores in Eight States - FDA Safety Alerts & Drug Recalls

In response to a recall by Satur Farms, Whole Foods Market is voluntarily recalling various prepared foods items in eight states containing baby spinach because of a potential contamination of Salmonella.

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

FDA statement from Commissioner Scott Gottlieb, M.D. announcing efforts to improve the quality of the information used to assess the effectiveness of REMS programs in supporting the safe use of medications - FDA Press Releases

FDA describes new policies to ensure the safe use of medications

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

Product Recall Because of Possible Health Risk - FDA Safety Alerts & Drug Recalls

Satur Farms, 3705 Alvah's Lane, Cutchogue, NY 11935 is voluntarily recalling Baby Spinach and Mesclun with the specific lot numbers listed below because it has the potential to be contaminated with Salmonella, an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people and others with weakened immune systems. Healthy persons infected with Salmonella often experience fever, diarrhea (which may be bloody), nausea, vomiting and abdominal pain.

from Food and Drug Administration--Recalls/Safety Alerts http://bit.ly/2CKjl1s
via IFTTT

General Mills Recalls Five Pound Bags of Gold Medal Unbleached Flour - FDA Safety Alerts & Drug Recalls

General Mills announced today a voluntary national recall of five-pound bags of its Gold Medal Unbleached Flour with a better if used by date of April 20, 2020. The recall is being issued for the potential presence of Salmonella which was discovered during sampling of the five-pound bag product.

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

Perrigo Issues Allergy Alert For Simple Truth Organic Banana, Strawberry & Apple Puree With Nonfat Greek Yogurt - FDA Safety Alerts & Drug Recalls

Perrigo Company, in coordination with The Kroger Company, is initiating a voluntary recall of one production lot of Simple Truth Organic Banana, Strawberry & Apple Fruit Puree with Nonfat Greek Yogurt (LOT L8159, best by 08/06/2019, produced in Spain) due to improper labeling that does not indicate the presence of milk, posing a potential risk to consumers with milk allergies.

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

FDA permits marketing of first test to aid in the diagnosis of a sexually-transmitted infection known as Mycoplasma genitalium - FDA Press Releases

FDA permits marketing of first test to aid in the diagnosis of a sexually-transmitted infection known as Mycoplasma genitalium

from Food and Drug Administration--Press Releases http://bit.ly/2B18EI2
via IFTTT

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

Torrent Pharmaceuticals Limited is expanding its voluntary recall from 10 lots of Losartan potassium tablets USP to include 6 lots of Losartan potassium and hydrochlorothiazide 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.

from Food and Drug Administration--Recalls/Safety Alerts http://bit.ly/2T8BdtZ
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 latest steps to strengthen FDA’s 510(k) program for premarket review of medical devices - FDA Press Releases

FDA takes more steps toward strengthening 510(k) program for premarket review of medical devices

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

Benzaldehyde thiosemicarbazone derivatives against replicating and nonreplicating Mycobacterium tuberculosis - Journal of Antibiotics

Benzaldehyde thiosemicarbazone derivatives against replicating and nonreplicating Mycobacterium tuberculosis

Benzaldehyde thiosemicarbazone derivatives against replicating and nonreplicating <i>Mycobacterium tuberculosis</i>, Published online: 21 January 2019; doi:10.1038/s41429-019-0140-9

Benzaldehyde thiosemicarbazone derivatives against replicating and nonreplicating Mycobacterium tuberculosis

from The Journal of Antibiotics - Issue - nature.com science feeds https://go.nature.com/2FKPjhc
via IFTTT

Ottogi America, Inc. Issues Allergy Alert on Undeclared Egg in Products - FDA Safety Alerts & Drug Recalls

Ottogi America, Inc. announced today it is recalling below 21 items due to a possibility of containing egg ingredient undeclared on the packages. People who have an allergy or severe sensitivity to eggs run the risk of serious or life-threatening allergic reaction of they consume these products.

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

Prinston Pharmaceutical Inc. issues Voluntary Nationwide Recall of Irbesartan and Irbesartan HCTZ Tablets Due to detection of a Trace Amount of Unexpected Impurity, N- nitrosodiethylamine (NDEA) in the Products - FDA Safety Alerts & Drug Recalls

-- Prinston Pharmaceutical Inc., dba Solco Healthcare LLC., has initiated a voluntary recall of one (1) lot of Irbesartan and seven (7) lots of Irbesartan HCTZ Tablets to the consumer level due to the detection of trace amount of an unexpected impurity found in an active pharmaceutical ingredient (API) manufactured by Zhejiang Huahai Pharmaceuticals.

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

Statement from FDA Commissioner Scott Gottlieb, M.D., on unprecedented new efforts to support development of over-the-counter naloxone to help reduce opioid overdose deaths - FDA Press Releases

FDA describes unprecedented new efforts to support development of over-the-counter naloxone to help reduce opioid overdose deaths

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

FDA approves first generic version of Sabril to help treat seizures in adults and pediatric patients with epilepsy - FDA Press Releases

FDA approved the first generic version of Sabril for treating complex partial seizures, as an adjunctive therapy in certain patients.

from Food and Drug Administration--Press Releases http://bit.ly/2QT7Olr
via IFTTT

Synthetic study of andrastins: stereoselective construction of the BCD-ring system - Journal of Antibiotics

Synthetic study of andrastins: stereoselective construction of the BCD-ring system

Synthetic study of andrastins: stereoselective construction of the BCD-ring system, Published online: 16 January 2019; doi:10.1038/s41429-018-0136-x

Synthetic study of andrastins: stereoselective construction of the BCD-ring system

from The Journal of Antibiotics - Issue - nature.com science feeds https://go.nature.com/2FD4rgQ
via IFTTT

RXBAR Recalls Certain Varieties of Bars Due to a Potential Undeclared Peanut Allergen - FDA Safety Alerts & Drug Recalls

RXBAR is voluntarily recalling certain varieties of bars because they may contain undeclared peanuts. People who have peanut allergies run the risk of serious or life-threatening allergic reaction if they consume this product.

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

Voluntary Recall Notice of El Guapo Chile Habanero and Chile Pasilla-Ancho Pouches Due to Unlabeled Peanut Allergen - FDA Safety Alerts & Drug Recalls

Mojave Foods Corporation is initiating a voluntary recall of El Guapo Chile Habanero and Chile Pasilla-Ancho pouches due to an unlabeled peanut allergen.

from Food and Drug Administration--Recalls/Safety Alerts http://bit.ly/2HdMd7L
via IFTTT

Statement from FDA Commissioner Scott Gottlieb, M.D. and Peter Marks, M.D., Ph.D., Director of the Center for Biologics Evaluation and Research on new policies to advance development of safe and effective cell and gene therapies - FDA Press Releases

FDA describes new policies to advance development of safe and effective cell and gene therapies

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

Stable isotope feeding studies reveal a steroid 5(6→7)abeo ring contraction biogenesis for the antibiotic solanioic acid produced by cultures of the fungus Rhizoctonia solani - Journal of Antibiotics

Stable isotope feeding studies reveal a steroid 5(6→7)abeo ring contraction biogenesis for the antibiotic solanioic acid produced by cultures of the fungus Rhizoctonia solani

Stable isotope feeding studies reveal a steroid 5(6→7)<i>abeo</i> ring contraction biogenesis for the antibiotic solanioic acid produced by cultures of the fungus <i>Rhizoctonia solani</i>, Published online: 11 January 2019; doi:10.1038/s41429-018-0137-9

Stable isotope feeding studies reveal a steroid 5(6→7)abeo ring contraction biogenesis for the antibiotic solanioic acid produced by cultures of the fungus Rhizoctonia solani

from The Journal of Antibiotics - Issue - nature.com science feeds https://go.nature.com/2FmO6NE
via IFTTT

Synthesis and characterization of NH2-(AEEA)n-amphotericin B derivatives - Journal of Antibiotics

Synthesis and characterization of NH₂-(AEEA)n-amphotericin B derivatives

Synthesis and characterization of NH₂-(AEEA)n-amphotericin B derivatives, Published online: 11 January 2019; doi:10.1038/s41429-018-0138-8

Synthesis and characterization of NH₂-(AEEA)n-amphotericin B derivatives

from The Journal of Antibiotics - Issue - nature.com science feeds https://go.nature.com/2FqUGlK
via IFTTT

Akazamicin, a cytotoxic aromatic polyketide from marine-derived Nonomuraea sp - Journal of Antibiotics

Akazamicin, a cytotoxic aromatic polyketide from marine-derived Nonomuraea sp

Akazamicin, a cytotoxic aromatic polyketide from marine-derived <i>Nonomuraea</i> sp, Published online: 10 January 2019; doi:10.1038/s41429-018-0139-7

Akazamicin, a cytotoxic aromatic polyketide from marine-derived Nonomuraea sp

from The Journal of Antibiotics - Issue - nature.com science feeds https://go.nature.com/2VK7rO6
via IFTTT

Antimicrobial anthraquinones from cultures of the ant pathogenic fungus Cordyceps morakotii BCC 56811 - Journal of Antibiotics

Antimicrobial anthraquinones from cultures of the ant pathogenic fungus Cordyceps morakotii BCC 56811

Antimicrobial anthraquinones from cultures of the ant pathogenic fungus <i>Cordyceps morakotii</i> BCC 56811, Published online: 09 January 2019; doi:10.1038/s41429-018-0135-y

Antimicrobial anthraquinones from cultures of the ant pathogenic fungus Cordyceps morakotii BCC 56811

from The Journal of Antibiotics - Issue - nature.com science feeds https://go.nature.com/2Qzlsdo
via IFTTT

Flupyranochromene, a novel inhibitor of influenza virus cap-dependent endonuclease, from Penicillium sp. f28743 - Journal of Antibiotics

Flupyranochromene, a novel inhibitor of influenza virus cap-dependent endonuclease, from Penicillium sp. f28743

Flupyranochromene, a novel inhibitor of influenza virus cap-dependent endonuclease, from <i>Penicillium</i> sp. f28743, Published online: 09 January 2019; doi:10.1038/s41429-018-0134-z

Flupyranochromene, a novel inhibitor of influenza virus cap-dependent endonuclease, from Penicillium sp. f28743

from The Journal of Antibiotics - Issue - nature.com science feeds https://go.nature.com/2VAPiC6
via IFTTT

Happy Together, Inc. Issues Voluntary Nationwide Recall of Product Due to Presence of Undeclared Sildenafil and Tadalafil - FDA Safety Alerts & Drug Recalls

Happy Together, Inc. Boynton Beach, FL is voluntarily recalling all lots within expiry of the Rhino 5k capsules to the consumer level. FDA analysis founds these products to be tainted with sildenafil and Tadalafil. Sildenafil/Tadalafil is an FDA approved drug for the treatment of erectile dysfunction, the presence of sildenafil in the Rhino 5k products renders them unapproved drugs for which safety and efficacy have not been established, therefor subject to recall.

from Food and Drug Administration--Recalls/Safety Alerts http://bit.ly/2VA7ewR
via IFTTT

Sun Pharmaceutical Industries, Inc. Issues Voluntary Nationwide Recall of Vecuronium Bromide for Injection Due to the Presence of Particulate Matter Identified as Glass - FDA Safety Alerts & Drug Recalls

Sun Pharmaceutical Industries, Inc. (SPII), a wholly owned subsidiary of Sun Pharmaceutical Industries, Ltd. is voluntarily recalling three lots of Vecuronium Bromide for Injection, 10 mg (lyophilized powder), and one lot of Vecuronium Bromide for Injection, 20 mg (lyophilized powder) to the hospital level. The Vecuronium Bromide for Injection has been found to contain particulate matter identified as glass.

from Food and Drug Administration--Recalls/Safety Alerts http://bit.ly/2Av6FeL
via IFTTT

Grand Strand Sandwich Company Recalls Lunch Box Sandwiches Italian Subs Lunch Box Sandwiches Ham & Swiss Croissants And Lunch Box Sandwiches Ham & Cheese Due To Possible Listeria Monocytogenes Contamination - FDA Safety Alerts & Drug Recalls

– Grand Strand Sandwich is recalling Lunch Box Italian Subs, Lunch Box Ham & Swiss Croissants and Lunch Box Ham & Cheese Frozen Wedges due to a potential contamination of Listeria Monocytogenes.

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

Statement from FDA Commissioner Scott Gottlieb, M.D., on the agency’s new actions under the Pre-Cert Pilot Program to promote a more efficient framework for the review of safe and effective digital health innovations - FDA Press Releases

FDA issues three documents that launch next phase of Pre-Cert Pilot Program to test new approaches for the review of digital health device applications.

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

Hy-Vee Voluntarily Recalls Cheesecakes Made with Diamond Crystal Mix - FDA Safety Alerts & Drug Recalls

Hy-Vee, Inc., based in West Des Moines, Iowa, is voluntarily recalling its cheesecakes made with Diamond Crystal Brands cheesecake mix due to the potential that they may be contaminated with Salmonella. The potential for contamination was brought to Hy-Vee’s attention today after receiving a letter from the supplier. The voluntary recall includes 32 varieties of cheesecakes in both 8-ounce and 32-ounce packages with best if used by dates of Dec. 6, 2018, through Jan. 11, 2019. No illnesses have been reported to date.

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

Author Index for Volume 71 - Journal of Antibiotics

Author Index for Volume 71

Author Index for Volume 71, Published online: 07 January 2019; doi:10.1038/s41429-018-0116-1

Author Index for Volume 71

from The Journal of Antibiotics - Issue - nature.com science feeds https://go.nature.com/2RaqKBo
via IFTTT

Substance Index for Volume 71 - Journal of Antibiotics

Substance Index for Volume 71

Substance Index for Volume 71, Published online: 07 January 2019; doi:10.1038/s41429-018-0119-y

Substance Index for Volume 71

from The Journal of Antibiotics - Issue - nature.com science feeds https://go.nature.com/2C2oguy
via IFTTT

Lupin Pharmaceuticals, Inc. Issues Voluntary Recall of Ceftriaxone for Injection USP, 250mg, 500mg, 1g and 2g - FDA Safety Alerts & Drug Recalls

Lupin Pharmaceuticals, Inc. is voluntarily recalling 5 lots of Ceftriaxone for Injection, USP, 250mg, 10 lots of Ceftriaxone for Injection, USP, 500mg, 24 lots of Ceftriaxone for Injection, USP, 1g and 3 lots of Ceftriaxone for Injection, USP 2g, to the hospital/physician level. The products have been found to contain visual grey particulate matter in reconstituted vials.

from Food and Drug Administration--Recalls/Safety Alerts http://bit.ly/2Qng50Y
via IFTTT

Olde York Potato Chips Issues Allergy Alert on Undeclared Milk in One Lot of Clancy's Wavy Potato Chips 10 Oz - FDA Safety Alerts & Drug Recalls

Olde York Potato Chips of Brampton, Ontario is recalling Clancy's Wavy Potato Chips 10 oz (UPC 0 41498 16306 8) with the specific lot code BEST If Used By FEB 22 19 1A6 because they 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. No other lot codes and no other products are involved in this action.

from Food and Drug Administration--Recalls/Safety Alerts http://bit.ly/2F7ROtU
via IFTTT

Shamrock Farms Issues Voluntary Recall of 2% Reduced Fat Vanilla Half Gallon Milk Due to Undeclared Almonds - FDA Safety Alerts & Drug Recalls

Shamrock Farms of Phoenix, Arizona is issuing a voluntary recall of Shamrock Farms 2% Reduced Fat Vanilla Half Gallon Milk with Best Before Date 3/16/2019. The recall comes after a product retain of Shamrock Farms 2% Reduced Fat Vanilla Half Gallon Milk with Use By 03/16/19 Time Stamp 08:18-11:13 04-05 #1, tested positive for an undeclared tree nut (almond) allergen.

from Food and Drug Administration--Recalls/Safety Alerts http://bit.ly/2R7xuzU
via IFTTT

Sequential exo-mode oxacyclizations for the synthesis of the CD substructure of brevenal - Journal of Antibiotics

Sequential exo-mode oxacyclizations for the synthesis of the CD substructure of brevenal

Sequential <i>exo</i>-mode oxacyclizations for the synthesis of the CD substructure of brevenal, Published online: 04 January 2019; doi:10.1038/s41429-018-0124-1

Sequential exo-mode oxacyclizations for the synthesis of the CD substructure of brevenal

from The Journal of Antibiotics - Issue - nature.com science feeds https://go.nature.com/2GPJEZs
via IFTTT

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

Torrent Pharmaceuticals Limited is expanding its voluntary recall from 2 lots of Losartan potassium tablets USP to a total of 10 lots, 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. Torrent is only recalling lots of losartan-containing products that contain N-nitrosodiethylamine (NDEA) above the acceptable daily intake levels released by the FDA.

from Food and Drug Administration--Recalls/Safety Alerts http://bit.ly/2F3huYB
via IFTTT

Results RNA LLC Issues Voluntary Worldwide/Nationwide Recall of Lubrisine Eye Drops Due to Manufacturing Sterility Concerns and Undeclared Colloidal Silver - FDA Safety Alerts & Drug Recalls

Results RNA LLC is voluntarily recalling Lubrisine Eye Drops to the healthcare practitioner, retail or consumer level. This product, in a recent FDA inspection, was found to be manufactured using practices that do not support its sterility and contained undeclared colloidal silver.

from Food and Drug Administration--Recalls/Safety Alerts http://bit.ly/2GOQ6zW
via IFTTT

Oskri Organics Corporation Recalls Oskri Organic Sunflower Butter Lot #099, Oskri Tahini Butter Lot #193 and Thrive Sunflower Butter Lot #233 Because of Possible Health Risk - FDA Safety Alerts & Drug Recalls

Oskri Organics Corporation of Lake Mills, WI is recalling Oskri Organic Sunflower Butter Lot # 099, Oskri Tahini Butter LOT # 193 and Thrive Sunflower Butter LOT # 233, because it has the potential to be contaminated with 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. 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 http://bit.ly/2RrIirV
via IFTTT