South Africa suspends 2 million Johnson & Johnson doses
Following a review of the FDA decision, the South African Health Products Regulatory Authority (SAHPRA) said in a statement that it had decided "not to release vaccine produced using the drug substance batches that were not suitable".

On Friday, the US Food and Drug Administration told J&J that millions of doses produced at the group's Emergent BioSolutions facility in the city of Baltimore were not suitable for use.
Following a review of the FDA decision, the South African Health Products Regulatory Authority (SAHPRA) said in a statement that it had decided "not to release vaccine produced using the drug substance batches that were not suitable".
J&J's Emergent plant was ordered to pause production in April several weeks after it was determined that batches of a substance used to produce the vaccine were cross-contaminated with ingredients from another jab made by Anglo-Swedish pharma giant AstraZeneca.
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