Baxter Healthcare Recalls ExactaMix Pro 1200 and Pro 2400 Due to a Software Error
Baxter Healthcare is recalling the ExactaMix Pro 1200 and Pro 2400 for a software error causing potential over-delivery of ingredients in the final solution.
Baxter Healthcare is recalling the ExactaMix Pro 1200 and Pro 2400 for a software error causing potential over-delivery of ingredients in the final solution.
Smiths Medical recalls Medfusion 3500 syringe pump due to software issues affecting delivery alarms, infusion restarts, screen locks, and critical functions.
EVair Air compressors recalled due to increased formaldehyde emissions at high temperature and low gas flow conditions when used with certain ventilators.
En combinaison avec la gemcitabine dans le traitement d'appoint du cancer du pancréas.
Megadyne issued a Class 1 Medical Device Correction to hospitals to limit the use of MEGA SOFT Universal and Universal Plus Reusable Patient Return Electrodes to patients aged 12 years or older after receiving reports of adult and pediatric patient burns following surgical procedures in which MEGA S
Problems may occur if electrical operating room table best practices are not followed. Read the FDA’s recommendations to avoid complications.
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