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ICU Medical Issues a Voluntary Nationwide Recall of Aminosyn II 15%, An Amino Acid Injection, Sulfite Free IV Solution Due to the Presence of Particulate Matter

ICU Medical, Inc. is voluntarily recalling one lot (2,112 units) of Aminosyn II, 15%, An Amino Acid Injection, Sulfite Free intravenous (IV) solution to the hospital/user level due to the presence of visible particulate matter identified as fibers, hair, and proteinaceous material along with other

http://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/icu-medical-issues-voluntary-nationwide-recall-aminosyn-ii-15-amino-acid-injection-sulfite-free-iv

 
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Primera semana de septiembre se convierte en la segunda con mayor cantidad de casos COVID-19

Primera semana de septiembre se convierte en la segunda con mayor cantidad de casos COVID-19

Primera semana de septiembre se convierte en la segunda con mayor cantidad de casos COVID-19Lunes 6 de setiembre, 2021. La semana epidemiológica 35 que abarcó del 29 de agosto al 4 de setiembre registró 16.601 casos de COVID-19...

https://www.ministeriodesalud.go.cr/index.php/centro-de-prensa/noticias/746-noticias-2021/2167-primera-semana-de-septiembre-se-convierte-en-la-segunda-con-mayor-cantidad-de-casos-covid-19

 
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Teligent Pharma, Inc.’s Issues Voluntary Recall of Lidocaine HCl Topical Solution 4% (Lot # 14218, Exp. 09/2022) Due to Super Potency

Teligent Pharma, Inc. is voluntarily recalling one lot of Lidocaine HCl Topical Solution 4%, 50ml in a screw cap glass bottle to the user level. The product is being recalled because the firms testing has found it to be super potent based on an Out of Specification (OOS) result obtained at the 18-m

http://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/teligent-pharma-incs-issues-voluntary-recall-lidocaine-hcl-topical-solution-4-lot-14218-exp-092022

 
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Magellan Diagnostics, Inc. Expands Voluntary Recall of LeadCare® Test Kits

Meridian Bioscience, Inc. (NASDAQ: VIVO), a provider of diagnostic testing solutions and life science raw materials, today announced its wholly owned subsidiary, Magellan Diagnostics, Inc. (“Magellan”), expanded the Class I recall of its LeadCare® II Blood Lead Test Kits, LeadCare Plus® Blood Lead T

http://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/magellan-diagnostics-inc-expands-voluntary-recall-leadcarer-test-kits

 
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Entidades nos invitan a escuchar y actuar en comunidad para prevenir el comportamiento suicida

Entidades nos invitan a escuchar y actuar en comunidad para prevenir el comportamiento suicida

Entidades nos invitan a escuchar y actuar en comunidad para prevenir el comportamiento suicida01 de setiembre del 2021. San José. Con el objetivo de sensibilizar a la población, abordar los estigmas y mitos que acompañan al comportamiento suicida...

https://www.ministeriodesalud.go.cr/index.php/centro-de-prensa/noticias/746-noticias-2021/2166-entidades-nos-invitan-a-escuchar-y-actuar-en-comunidad-para-prevenir-el-comportamiento-suicida

 
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Janus Kinase (JAK) inhibitors: Drug Safety Communication – FDA Requires Warnings about Increased Risk of Serious Heart-related Events, Cancer, Blood Clots, and Death

FDA is requiring revisions to the Boxed Warning, FDA’s most prominent warning, for Xeljanz/Xeljanz XR, Olumiant, and Rinvoq to include information about the risks of serious heart-related events, cancer, blood clots, and death.

http://www.fda.gov/safety/medical-product-safety-information/janus-kinase-jak-inhibitors-drug-safety-communication-fda-requires-warnings-about-increased-risk