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Fresenius Kabi Issues Voluntary Recall of Sodium Acetate Injection, USP Due to the Presence of Particulate Matter

Fresenius Kabi USA is voluntarily recalling seven lots of Sodium Acetate Injection, USP, 400 mEq/100 mL (4 mEq/mL), 100 mL fill in a 100 mL vial to the user level due to the presence of particulate matter found in reserve and/or stability sample vials. Microscopic and elemental analyses determined t

http://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/fresenius-kabi-issues-voluntary-recall-sodium-acetate-injection-usp-due-presence-particulate-matter

 
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B. Braun Medical Inc. Issues Voluntary Nationwide Recall of 0.9% Sodium Chloride for Injection USP 250ML in Excel Due to Fluid Leakage or Low Fill Volume

B. Braun Medical Inc. (B. Braun) is voluntarily recalling five (5) lots of 0.9% Sodium Chloride for Injection USP 250ML in Excel within the United States to the hospital/user level.

http://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/b-braun-medical-inc-issues-voluntary-nationwide-recall-09-sodium-chloride-injection-usp-250ml-excel

 
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Salud recuerda obligatoriedad de tercera dosis de vacuna Covid-19 para funcionarios públicos

Salud recuerda obligatoriedad de tercera dosis de vacuna Covid-19 para funcionarios públicos

 Salud recuerda obligatoriedad de tercera dosis de vacuna Covid-19 para funcionarios públicos28 de febrero del 2022. El Ministerio de Salud recuerda a las entidades públicas la vigencia del Decreto Ejecutivo N° 43249-S de 7 de octubre de 2021

https://www.ministeriodesalud.go.cr/index.php/centro-de-prensa/noticias/749-noticias-2022/2283-salud-recuerda-obligatoriedad-de-tercera-dosis-de-vacuna-covid-19-para-funcionarios-publicos

 
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FDA Advisory Panel Recommendations on Lifelong Surveillance and Long-Term Postmarket Data Collection for Patients with AAA Endovascular Aortic Repair – Letter to Health Care Providers

Regular clinical follow-up and imaging is critical to detect EVAR device and treatment failures.

http://www.fda.gov/medical-devices/letters-health-care-providers/fda-advisory-panel-recommendations-lifelong-surveillance-and-long-term-postmarket-data-collection

 
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Plan Nacional fortalecerá la prevención, vigilancia y control de enfermedades transmitidas por vectores

Plan Nacional fortalecerá la prevención, vigilancia y control de enfermedades transmitidas por vectoresn

Plan Nacional fortalecerá la prevención, vigilancia y control de enfermedades transmitidas por vectores 25 de febrero, 2022. El Ministerio de Salud en conjunto con la Organización Panamericana de la Salud (OPS)

https://www.ministeriodesalud.go.cr/index.php/centro-de-prensa/noticias/746-noticias-2021/2282-plan-nacional-fortalecera-la-prevencion-vigilancia-y-control-de-enfermedades-transmitidas-por-vectores

 
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Antibody Testing Is Not Currently Recommended to Assess Immunity After COVID-19 Vaccination: FDA Safety Communication

FDA reminds the public and health care providers that results from currently authorized SARS-CoV-2 antibody tests should not be used to evaluate a person’s level of immunity from COVID-19 at any time, and especially after the person received a COVID-19 vaccination.

http://www.fda.gov/medical-devices/safety-communications/antibody-testing-not-currently-recommended-assess-immunity-after-covid-19-vaccination-fda-safety