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.
from Top Health News | Latest Health & Healthcare Industry Information and Updates: ET HealthWorld : ETHealthworld.com https://ift.tt/csHT1Bq
Home »
Top Health News | Latest Health & Healthcare Industry Information and Updates: ET HealthWorld : ETHealthworld.com
» Recall of iron supplement by Maharashtra FDA remains only on paper
https://ift.tt/43nTYLZ
No comments:
Post a Comment