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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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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.
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Pfizer Voluntary Nationwide Recall of Lots of ACCUPRIL® (Quinapril HCl) Due to N-Nitroso-Quinapril Content
Pfizer is voluntarily recalling five (5) lots of Accupril (Quinapril HCl) tablets distributed by Pfizer to the patient (consumer/user) level due to the presence of a nitrosamine, Nnitroso-quinapril, observed in recent testing above the Acceptable Daily Intake (ADI) level.
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Genetic Non-Invasive Prenatal Screening Tests May Have False Results: FDA Safety Communication
Pregnant patients should discuss test results with a health care provider before making any decisions about their pregnancy
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Mylan Pharmaceuticals Inc., a Viatris Company, Conducting Voluntary Nationwide Recall of One Batch of Insulin Glargine (Insulin glargine-yfgn) Injection, 100 units/mL (U-100), Due to the Potential for a Missing Label in the Batch
Mylan Pharmaceuticals Inc., a Viatris company, is voluntarily recalling one batch of its Insulin Glargine (Insulin glargineyfgn) Injection, 100 units/mL (U-100), which is packaged in a 10 mL vial that is inside a carton. This product is not the branded Semglee vial but the unbranded Insulin Glargine
