Categories 14th Annual PQT Medicines Quality Assessment Training
1st Biotherapeutic Product (BTP) and Similar Biotherapeutic Product (SBP) assessment training
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Philips Respironics CPAP, BiPAP, and Ventilator Recalls: Frequently Asked Questions
Find answers to frequently asked questions on Philips Respironics ventilators, BiPAP, and CPAP machines recall
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Philips Respironics Issues Voluntary Recall Notification/Field Safety Notice* for the V60 Ventilator Product Family
Royal Philips (NYSE: PHG, AEX: PHIA), a global leader in health technology, today announced that its subsidiary Philips Respironics is notifying customers of its V60/V60 Plus and V680 ventilators about a potential issue with the electrical circuit in these ventilators that controls the 35V power sup
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Fagron Inc. Issues Voluntary Nationwide Recall of SyrSpend SF Cherry Due to Microbial Contamination
St. Paul, Minnesota, Fagron Inc. (“Fagron”) is voluntarily recalling two lots of SyrSpend SF Cherry to the hospital, pharmacy, and distributor level out of an abundance of caution. The affected lots are potentially contaminated with Burkholderia gladioli. Burkholderia gladioli is an opportunistic pa
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Stop New Implants of the Medtronic HVAD System – Letter to Health Care Providers
Medtronic has stopped the sale and distribution of HVAD because the internal pump may delay or fail to restart.
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Celltrion USA Recalls Certain Point of Care DiaTrust COVID-19 Ag Rapid Test Kits Which May Have Been Distributed to Unauthorized, Non-CLIA-Certified Users
COVID-19 Ag Rapid Tests are being recalled because they may have been distributed to unauthorized, non-CLIA-certified users.
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Radiothérapie adjuvante pour le traitement du cancer du sein de stade précoce: efficacité et innocuité d’une irradiation complète du sein en 5 fractions (ultrahypofractionnement)
Radiothérapie adjuvante pour le traitement du cancer du sein de stade précoce: efficacité et innocuité d’une irradiation complète du sein en 5 fractions (ultrahypofractionnement)
https://sites.bvsalud.org/redetsa/brisa/resource/?id=biblioref.referencesource.1367477
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Potential Risk of Airway Obstruction When Using Certain Electromyogram Endotracheal Tubes – Letter to Health Care Providers
The FDA has received reports of airway obstruction and ventilation failure for certain EMG endotracheal tubes.
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Molnupiravir para el tratamiento de pacientes con COVID-19: 19 de abril de 2022
Molnupiravir para el tratamiento de pacientes con COVID-19: 19 de abril de 2022
https://sites.bvsalud.org/redetsa/brisa/resource/?id=biblioref.referencesource.1367179
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Medtronic Recalls Harmony Delivery Catheter, Part of Transcatheter Pulmonary Valve (TPV) System, for Risk of Capsule Break During Use
The capsule at the end of the delivery catheter used to place Harmony’s pulmonary valve may come loose during placement due to a bond break.
