Blog – Page 30 – PRAIS 2.0

BD (Becton, Dickinson and Company) today announced the voluntary recall of one lot of ChloraPrep™ Clear 1 mL Applicators due to fungal contamination under certain environmental conditions allowing the growth of Aspergillus penicillioides

http://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/bd-announces-voluntary-worldwide-recall-one-lot-chlorapreptm-clear-1-ml-applicators-due-fungal

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OPAS e Ministério da Saúde do Brasil reúnem países da América Latina para catalisar eliminação de doenças transmissíveis em contextos de privação de liberdade

admin - 20:03, 13 de February de 2025213

Latin American countries aim to eliminate infectious diseases in prisons

Oscar Reyes

14 Feb 2025

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FDA Approves First Rapid-Acting Insulin Biosimilar Product for Treatment of Diabetes

Murilo Freitas - 19:59, 13 de February de 2025201

FDA Approves First Rapid-Acting Insulin Biosimilar Product for Treatment of Diabetes
http://www.fda.gov/news-events/press-announcements/fda-approves-first-rapid-acting-insulin-biosimilar-product-treatment-diabetes

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Nueva guía de la OPS busca mejorar la detección temprana y las tasas de supervivencia del cáncer infantil en América Latina y el Caribe

admin - 15:09, 13 de February de 2025264

New PAHO guide aims to improve early detection and survival rates of childhood cancer in Latin America and the Caribbean

Cristina Mitchell

14 Feb 2025

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Heart Pump Recall: Abiomed, Inc. Updates Use Instructions for Impella RP with SmartAssist and Impella RP Flex with SmartAssist Due to A Risk That the Tip of Guidewires or Other Medical Devices May Come into Contact with The Impella Pump During Insertion, Adjustment, Or Removal

Murilo Freitas - 05:00, 13 de February de 2025225

Heart Pump Recall: Abiomed, Inc. Updates Use Instructions for Impella RP with SmartAssist and Impella RP Flex with SmartAssist Due to A Risk That the Tip of Guidewires or Other Medical Devices May Come into Contact with The Impella Pump During Insertion, Adjustment, Or Removal

http://www.fda.gov/medical-devices/medical-device-recalls/heart-pump-recall-abiomed-inc-updates-use-instructions-impella-rp-smartassist-and-impella-rp-flex

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ICU Medical Issues Nationwide Recall of Potassium Chloride Injection, 20 mEq and Potassium Chloride Injection, 10 mEq Due to Mislabeling

Murilo Freitas - 05:00, 13 de February de 2025205

ICU Medical, Inc. is voluntarily recalling one lot each of POTASSIUM CHLORIDE Inj. bags with overwrap labels 10mEq, packaged in cases of POTASSIUM CHLORIDE Inj. 20 mEq, to the user level. ICU medical has received a customer complaint which states that bags of POTASSIUM CHLORIDE Inj. 20 mEq have inco

http://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/icu-medical-issues-nationwide-recall-potassium-chloride-injection-20-meq-and-potassium-chloride