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American Health Packaging Issues Voluntary Nationwide Recall of Ranitidine Syrup (Ranitidine Oral Solution USP) 150 mg/10 mL Liquid Unit Dose Cups Due to the Detection of N-nitrosodimethylamine (NDMA) Impurity

Murilo Freitas - 05:00, 7 de noviembre de 2019439
American Health Packaging is voluntarily recalling eight lots of Ranitidine Syrup (Ranitidine Oral Solution USP) 150 mg/10 mL Liquid Unit Dose Cups to the consumer level due to the detection of trace amounts of an unexpected impurity found in the finished drug product. The impurity detected in the f

http://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/american-health-packaging-issues-voluntary-nationwide-recall-ranitidine-syrup-ranitidine-oral

 
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Philips Medical Systems (Cleveland) Recalls Forte Gamma Camera System Due to Potential for the Detector to Become Detached

Murilo Freitas - 13:00, 6 de noviembre de 2019608
The detector on the Forte Gamma Camera System has the potential to become detached without warning which could result in a serious injury or death.

http://www.fda.gov/medical-devices/medical-device-recalls/philips-medical-systems-cleveland-recalls-forte-gamma-camera-system-due-potential-detector-become

 
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Costa Rica fortalece ruta hacia la eliminación de la malaria

Murilo Freitas - 21:52, 5 de noviembre de 2019513

Costa Rica fortalece ruta hacia la eliminación de la malaria

Costa Rica fortalece ruta hacia la eliminación de la malaria6 noviembre del 2019. El Ministerio de Salud, la Caja Costarricense de Seguro Social y el Instituto Costarricense de Investigación, Enseñanza en Nutrición y Salud (INCIENSA) desarrollan una serie de acciones encaminadas…

https://www.ministeriodesalud.go.cr/index.php/noticias/noticias-2019/1504-costa-rica-fortalece-ruta-hacia-la-eliminacion-de-la-malaria

 
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Abbott Recalls CentriMag Circulatory Support System Motor Due to Pump and Motor Issues

Murilo Freitas - 05:00, 5 de noviembre de 2019570
Abbott is recalling their CentriMag System due to a calibration system error resulting from electromagnetic interference (EMI) that may cause low or no flow from the device, the console screen to blank, and various inaccurate alarms.

http://www.fda.gov/medical-devices/medical-device-recalls/abbott-recalls-centrimag-circulatory-support-system-motor-due-pump-and-motor-issues

 
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