Urgent
Santé·23/05/2026Résumé IA
FDA Classifies Recall of 'Neveronix' Multivitamin
The FDA has classified the recall of over 4,000 bottles of 'Neveronix' multivitamin, produced by Lorenz Pharmaceuticals International, as Class II. The product, containing B vitamins, C, and folic acid, was sold between February and May 2026 in several US states and Puerto Rico.
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RT عربي1 min de lecture