Eitan Medical Ltd Recalls Sapphire Infusion Pumps for Failure to Detect Air in the Line
Sapphire Infusion Pumps are being recalled because they may fail to detect air in the line. The failure could cause injury or death.
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Sapphire Infusion Pumps are being recalled because they may fail to detect air in the line. The failure could cause injury or death.
BD/Carefusion 303 is recalling their Alaris Infusion Pumps to make a correction on compatibility issues with Cardinal Health Monoject syringes.
Chez les patients ayant commencé à présenter des réactions d'hypersensibilité aux taxanes.
Consider using plastic syringes not manufactured in China, if possible.
Baxter International Inc. announced today it has issued an Urgent Medical Device Correction for the Novum IQ syringe infusion pump. The Correction is due to the potential for an incomplete infusion following one or more downstream occlusion alarms. Baxter notified impacted customers in October and i
E. Hampton NY- Meta Herbal is voluntarily recalling 500 blister packs of Magnum XXL 9800 2000 mg per capsule, to the consumer level. The products have been found to be tainted with Sildenafil. Sildenafil is an ingredient known as a Phosphodiesterase Inhibitor (PDE-5) found in FDA-approved products f
Reports of smoke, sparks, fire, and burns stemming from use of the DreamStation2 CPAP machines prompt warning from the FDA.
The FDA is warning that the antiseizure medicines can cause a rare but serious reaction, called Drug Reaction with Eosinophilia and Systemic Symptoms (DRESS), that can be life-threatening if not diagnosed and treated quickly.
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