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F&S Medical Supply, DBA Pink Toyz Issues Voluntary Nationwide Recall of Pink Pussycat Capsules Due to the Presence of Undeclared Sildenafil

Murilo Freitas - 04:00, 31 de marzo de 2022295
Chatsworth, California, F&S Medical Supply, dba Pink Toyz is voluntarily recalling one lot of Pink Pussycat 3000 mg capsules to the consumer level. FDA analysis has found the product Pink Pussycat to be tainted with sildenafil, an ingredient known as a phosphodiesterase (PDE-5) inhibitor found in an

http://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/fs-medical-supply-dba-pink-toyz-issues-voluntary-nationwide-recall-pink-pussycat-capsules-due

 
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Best Brand Consumers Products, Inc. Issues Voluntary Recall of Mickey Mouse Hand Sanitizer Ethyl Alcohol 68% Due to Presence of Methanol and the Mandalorian Hand Sanitizer Ethyl Alcohol 68% Due to the Presence of Benzene

Murilo Freitas - 04:00, 31 de marzo de 2022293
Best Brands Consumer Products, Inc. is voluntarily recalling two (2) finished product lots of The Mandalorian Hand Sanitizer Ethyl Alcohol 68%, available in green and blue formulations and Mickey Mouse Hand Sanitizer Ethyl Alcohol 68% blue formulation to the consumer level.

http://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/best-brand-consumers-products-inc-issues-voluntary-recall-mickey-mouse-hand-sanitizer-ethyl-alcohol

 
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Iodine-Containing Contrast Media: Drug Safety Communication – FDA Recommends Thyroid Monitoring in Babies and Young Children Who Receive Injections of Iodine-Containing Contrast Media for Medical Imaging

Murilo Freitas - 20:56, 29 de marzo de 2022256
The FDA is recommending that newborns and children through 3 years old have follow-up thyroid monitoring within 3 weeks after receiving injections of contrast media containing iodine, also called “contrast dye,” for X-rays and other medical imaging procedures.

http://www.fda.gov/safety/medical-product-safety-information/iodine-containing-contrast-media-drug-safety-communication-fda-recommends-thyroid-monitoring-babies

 
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A 10 años de vigencia de la Ley General de Control de Tabaco, Costa Rica continúa su lucha contra este flagelo

Murilo Freitas - 19:47, 29 de marzo de 2022317

A 10 años de vigencia de la Ley General de Control de Tabaco, Costa Rica continúa su lucha contra este flagelo

A 10 años de vigencia de la Ley General de Control de Tabaco, Costa Rica continúa su lucha contra este flageloMiércoles 30 de marzo, 2022. Luego de 10 años de haber sido aprobada la Ley General de Control de Tabaco en Costa Rica, Ley 9028…

https://www.ministeriodesalud.go.cr/index.php/centro-de-prensa/noticias/749-noticias-2022/2299-a-10-anos-de-vigencia-de-la-ley-general-de-control-de-tabaco-costa-rica-continua-su-lucha-contra-este-flagelo

 
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Unilever Issues Voluntary Nationwide Recall of Suave 24-Hour Protection Aerosol Antiperspirant Powder and Suave 24-Hour Protection Aerosol Antiperspirant Fresh Due to Presence of Slightly Elevated Levels of Benzene

Murilo Freitas - 04:00, 29 de marzo de 2022295
Unilever United States is voluntarily recalling two Suave 24-Hour Protection Aerosol Antiperspirants to the consumer level. An internal review showed slightly elevated levels of benzene in some product samples. While benzene is not an ingredient in any of the recalled products, the review showed tha

http://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/unilever-issues-voluntary-nationwide-recall-suave-24-hour-protection-aerosol-antiperspirant-powder

 
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Teva Issues Voluntary Nationwide Recall of One Lot of IDArubicin Hydrochloride Injection USP 5 mg/5 mL Due to the Presence of Particulate Matter

Murilo Freitas - 04:00, 28 de marzo de 2022269
Teva Pharmaceuticals has initiated a voluntary nationwide recall of lot 31329657B of IDArubicin Hydrochloride Injection USP 5 mg/5 mL vial, to the user level in the United States. This voluntary recall is initiated based on an internal inspection that found particulate matter in one vial of the prod

http://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/teva-issues-voluntary-nationwide-recall-one-lot-idarubicin-hydrochloride-injection-usp-5-mg5-ml-due

 
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