Recall of iron supplement by Maharashtra FDA remains only on paper

On November 17, the FDA issued an order asking Emcure to recall its product Orofer's (batch no. ELF8BB2001) following the death of a 55-year-old man at Saifee Hospital due to a suspected adverse drug reaction. Eight days after the state Food and Drug Administration (FDA) recalled a batch of the iron supplement infection Orofer FCM over safety concerns, not a single vial has returned to the manufacturer or the distributors.

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