Blog – Page 39 – PRAIS 2.0

The Perseus A500 that provides anesthesia and/or ventilation during surgical or diagnostic procedures may unexpectedly shutdown while using battery power.

http://www.fda.gov/medical-devices/medical-device-recalls/draeger-inc-recalls-perseus-a500-anesthesia-system-risk-sudden-unexpected-shutdown-when-used-battery

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BioMérieux Inc. Recalls VITEK 2 AST Kit due to Incorrect Ceftriaxone Concentrations

Murilo Freitas - 04:00, 14 de May de 2024392

BioMérieux is recalling their VITEK 2 AST cards, used for testing bacterial sensitivity to antibiotics, due to excessive Ceftriaxone in two wells.

http://www.fda.gov/medical-devices/medical-device-recalls/biomerieux-inc-recalls-vitek-2-ast-kit-due-incorrect-ceftriaxone-concentrations

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FDA Roundup: May 14, 2024

Murilo Freitas - 17:51, 13 de May de 2024418

FDA Roundup: May 14, 2024
http://www.fda.gov/news-events/press-announcements/fda-roundup-may-14-2024

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GAFFI and PAHO Join Forces to Combat Fungal Disease in Latin America and the Caribbean

admin - 10:00, 13 de May de 2024258

GAFFI and PAHO Join Forces to Combat Fungal Disease in Latin America and the Caribbean

Cristina Mitchell

14 May 2024

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Philips Respironics, Inc. Recalls Trilogy Evo Continuous Ventilators due to a Software-Related Possible Power Malfunction

Murilo Freitas - 04:00, 12 de May de 2024279

Philips Respironics is recalling their Trilogy Evo ventilators due to a software-related possible power malfunction, leading to a sudden loss of ventilation.

http://www.fda.gov/medical-devices/medical-device-recalls/philips-respironics-inc-recalls-trilogy-evo-continuous-ventilators-due-software-related-possible