Tag: medwatch
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Global Mix Recalls Niwali Tejocote Capsules and Pieces Over Yellow Oleander Contamination
Global Mix recalls niwali Tejocote Capsules and Pieces nationwide after FDA found the products appear to be toxic yellow oleander, which can cause severe or fatal health effects.
HealthBusinessLaw EnforcementUSAMedical ScienceSocial Issues Product RecallGlobal Mixniwali Tejocote Capsulesniwali Tejocote Piecesyellow oleanderFDAMedWatchFood RecallsDrugs
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Par Health Recalls Two Lots of Dexmedetomidine Injection Over Particulate Matter
Par Health is recalling two lots of Dexmedetomidine HCl in 0.9% Sodium Chloride Injection to the hospital level after cellulose or stopper material was found in the product.
HealthBusinessLaw EnforcementUSAMedical ScienceLegalSocial Issues Product RecallDexmedetomidine HClPar HealthUS Food and Drug AdministrationParticulate MatterMedWatchSodium Chloride InjectionFood RecallsFDADrugs
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Otsuka ICU Medical Recalls Sodium Chloride Injection Lot Over Potassium Chloride Mix-Up
Otsuka ICU Medical recalls one lot of 0.9% Sodium Chloride Injection after a customer found a highly concentrated Potassium Chloride bag inside the overwrap, warning of potentially fatal outcomes.
HealthBusinessLaw EnforcementMedical ScienceLegalSocial Issues Product RecallOtsuka ICU Medical0.9% Sodium Chloride InjectionPotassium Chloride InjectionUS Food and Drug AdministrationMedWatchIntravenousFood RecallsFDADrugs
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A&P Creations Recalls X10 Natural Enhancement Supplement Over Undeclared Viagra and Cialis Ingredients
A&P Creations is recalling X10 Natural Enhancement Supplement after undeclared sildenafil and tadalafil were found in the product, which was sold nationwide through Amazon, Walmart.com and naturefuel.us.
HealthBusinessLaw EnforcementUSAMedical ScienceLegalSocial Issues Product RecallA&P CreationsX10 Natural Enhancement SupplementSildenafilTadalafilUS Food and Drug AdministrationMedWatchFood RecallsFDADrugs
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Q’Apel Medical Recalls and Discontinues 072 Aspiration System (Hippo)
Q’Apel Medical Inc. recalls 1,617 units of its 072 Aspiration System (Hippo) due to concerns about the distal tip design. The company has chosen to discontinue the product line.
HealthScience & TechnologyMedical ScienceFederal GovernmentLegalAsia Q’Apel Medical Inc.072 Aspiration SystemHippoProduct RecallFDAMedical DeviceMedWatch