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recall
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South Africa recalls four batches of Arya Pharma Enalapril 10 mg over failed quality tests
Arya Pharma is implementing the Class II Type A recall in consultation with Sahpra and in accordance with the Medicines and Related Substances Act 101 of 1965, as amended.
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Lupin recalls 2.5M prednisolone eye drop bottles in United States due to foreign substance concerns
The FDA has classified the action as a Class II recall, indicating that the affected product may cause temporary or medically reversible adverse health effects, although the likelihood of serious health consequences remains low.