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
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Tuesday, January 8, 2019
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
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from Food and Drug Administration--Recalls/Safety Alerts http://bit.ly/2Av6FeL
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Monday, January 7, 2019
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
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from Food and Drug Administration--Recalls/Safety Alerts http://bit.ly/2FhDwqp
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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
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from Food and Drug Administration--Press Releases http://bit.ly/2RaEWdH
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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
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from Food and Drug Administration--Recalls/Safety Alerts http://bit.ly/2LTCqCL
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Sunday, January 6, 2019
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
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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
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