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FDA Warns Against Purchasing or Using Chemical Peel Skin Products Without Professional Supervision fda.gov/drugs/drug-saf…

FDA Warns Consumers Not to Use Optimized Plant Mediated Solutions (OPMS) Black Liquid Kratom fda.gov/food/alerts-ad…

Ambulatory Infusion Pump Software Correction: Smiths Medical Issues Correction for CADD-Solis and CADD-Solis VIP Ambulatory Infusion Pump Software due to Multiple Issues Related to Outdated Software fda.gov/medical-device…

Nerve Monitoring System Correction: Medtronic Issues Correction for NIM Vital Nerve Monitoring System due to the Potential for False Negative Response fda.gov/medical-device…

One Lot of Heparin Sodium 0.9% Sodium Chloride Injection by Baxter: Recall - Due to Potential for Elevated Endotoxin Levels fda.gov/safety/recalls…

0.9% Sodium Chloride for Injection USP, 1000 mL in E3 Containers by B. Braun: Recall - Due to the Potential for Particulate Matter and Leakage fda.gov/safety/recalls…

One Batch of Premium Infant Formula with Iron Milk-Based Powder by Perrigo: Recall - Due to Elevated Levels of Vitamin D fda.gov/safety/recalls…

FDA Warns Consumers to Not Purchase or Use Unapproved Inhalant Products Marketed for Alertness and Energy Boosting: CDER Alert fda.gov/drugs/drug-saf…

Infusion Pump Battery Correction: ICU Medical Updates Instructions for Use Regarding Batteries in Plum 360, A+ and A+3 Infusion System due to Diminished Battery Life that May Impact Infusion Delivery fda.gov/medical-device…

Endurance Pro Capsules by Veata: Recall - Due to the Potential Presence of Undeclared Sildenafil fda.gov/safety/recalls…

Boom Max Capsules by Boulla: Recall - Due to the Potential Presence of Undeclared Sildenafil fda.gov/safety/recalls…

Chest Compression Device Recall: Defibtech, LLC, Removes RMU-2000 ARM XR Chest Compression Device due to Risk of Device Stopping Compressions fda.gov/medical-device…

Diamond Shruumz-Brand Chocolate Bars, Cones, & Gummies: Investigation of Illnesses - Do Not Eat, Sell, or Serve Any Flavor of Diamond Shruumz- Brand Chocolate Bars, Cones, and Gummies. An Updated Retailer List and Additional Sample Results Are Available. fda.gov/food/outbreaks…

Clot Removal Device Correction: Inari Medical Updates ClotTriever XL Use Instructions fda.gov/medical-device…

Tattoo Pigments by Sierra Stain: Recall - Because of Possible Health Risk fda.gov/safety/recalls…

Update:Tandem Diabetes Care, Inc. Recalls Version 2.7 of the Apple iOS t:connect Mobile App Used in Conjunction with t:slim X2 Insulin Pump with Control-IQ Technology Prompted by a Software Problem Leading to Pump Battery Depletion fda.gov/medical-device…

Lung Therapy Component Recall: Baxter Healthcare Corporation Recalls Certain Volara System Single-Patient Use Circuits and Blue Ventilator Adapter Assemblies Due to Disconnection Risk That May Prevent Proper Ventilation fda.gov/medical-device…

Laryngoscope Recall: Medtronic Removes Certain McGrath MAC Video Laryngoscopes, Updates Use Instructions for Others due to Increased Risk for Battery Overheat and Explosion fda.gov/medical-device…

Continuous Glucose Monitoring Sensor Recall: Abbott Diabetes Care Inc. Issues Recall for Certain FreeStyle Libre 3 Sensors due to Risk for Inaccurate High Glucose Readings fda.gov/medical-device…

Ventilator Correction: Breas Medical Updates Use Instructions for Vivo 45 LS due to Potential Risk of Elevated Formaldehyde Exposure in New Ventilators fda.gov/medical-device…