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S&B Shopper LLC Issues Voluntary Nationwide Recall of Imperial Extreme 2000mg Due to Presence of Undeclared Sildenafil and Tadalafil

Murilo Freitas - 04:00, 24 de marzo de 2021427
S&B Shopper LLC is voluntarily recalling all lots of Imperial Extreme 2000mg capsules, to the consumer level. FDA analysis has found this product to contain undeclared sildenafil and tadalafil. Sildenafil and tadalafil are ingredients known as phosphodiesterase (PDE-5) inhibitors found in FDA approv

http://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/sb-shopper-llc-issues-voluntary-nationwide-recall-imperial-extreme-2000mg-due-presence-undeclared

 
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Costa Rica continúa como candidata para la eliminación de la tuberculosis al 2035

Murilo Freitas - 22:03, 23 de marzo de 2021597

Costa Rica continúa como candidata para la eliminación de la tuberculosis al 2035

Costa Rica continúa como candidata para la eliminación de la tuberculosis al 2035San José, 24 de marzo de 2021. Pese a que la tuberculosis es una de las infecciones que más muertes provoca a nivel mundial …

https://www.ministeriodesalud.go.cr/index.php/centro-de-prensa/noticias/746-noticias-2021/2075-costa-rica-continua-como-candidata-para-la-eliminacion-de-la-tuberculosis-al-2035

 
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Medtronic Recalls Affinity Pixie™ Oxygenator and Cardiotomy/Venous Reservoir with Balance™ Biosurface for Possible High Levels of Endotoxins

Murilo Freitas - 04:00, 23 de marzo de 2021405
Affinity Pixie Oxygenator and CVR are used in pediatric patients for cardiopulmonary bypass. Affected devices may cause more exposure to endotoxins.

http://www.fda.gov/medical-devices/medical-device-recalls/medtronic-recalls-affinity-pixietm-oxygenator-and-cardiotomyvenous-reservoir-balancetm-biosurface

 
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Alembic Pharmaceuticals Limited Issues Voluntary Nationwide Recall of Telmisartan Tablets, USP, 20 mg Due to Label Mix-Up

Murilo Freitas - 04:00, 23 de marzo de 2021616
Bridgewater, NJ, Alembic Pharmaceuticals, Inc is voluntarily recalling one lot of Telmisartan Tablets, USP, 20 mg, packaged in 30-count bottles, Lot No. 1905005661 to the consumer level. The product is being recalled due to a market complaint received which stated that one bottle labelled as 30-cou

http://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/alembic-pharmaceuticals-limited-issues-voluntary-nationwide-recall-telmisartan-tablets-usp-20-mg-due

 
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Durisan Hand Sanitizer Recall Due to Microbial Contamination

Murilo Freitas - 04:00, 23 de marzo de 2021458
Sanit Technologies LLC d/b/a Durisan announces a voluntary recall of the lots listed in the table below of Durisan Antimicrobial Hand Sanitizer, Non-Alcohol products in various sizes listed. The products are being recalled due to microbial contamination. Specifically, out of specification results fo

http://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/durisan-hand-sanitizer-recall-due-microbial-contamination

 
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