Tag: sodium_chloride
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FDA Issues Early Alert for AVID Medical Kits Containing Recalled Sodium Chloride
AVID Medical convenience kits contain recalled sodium chloride ampules, raising sterility and quality concerns. The FDA issued an "Early Alert" due to potential risks of infection and severe complications, especially for critically ill patients and spinal procedures.
HealthBusinessScience & TechnologyMedical ScienceLegalEducation AVID MedicalSodium ChlorideMedical Device RecallFDAHuons Co., Ltd.Spectra Medical DevicesEpidural KitsFood RecallsDrugs
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FDA Alerts Public to Recalled Components in Medical Action Industries Epidural Kits
Medical Action Industries epidural kits may contain recalled Huons Co., Ltd. sodium chloride ampules, posing risks like infection, organ failure, and paralysis. The FDA is aware, and customers are advised to correct kits before use.
HealthBusinessMedical ScienceFederal GovernmentSocial Issues Epidural KitsMedical Action IndustriesSodium ChlorideProduct RecallHuons Co., Ltd.FDAMedical DevicesFood RecallsDrugs
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FDA Issues Early Alert for Becton Dickinson Kits with Recalled Sodium Chloride
FDA issues an Early Alert for Becton Dickinson convenience kits containing recalled Huons Co., Ltd. sodium chloride ampules. Patients face infection risks from compromised sterility, though no serious injuries are reported yet.
HealthBusinessPolitics and GovernmentUSAMedical ScienceFederal GovernmentLegal Becton DickinsonFDAMedical Device RecallConvenience KitsSodium ChlorideHuons Co., Ltd.Patient SafetyFood RecallsDrugs