The US Food and Drug Administration said Friday it had told Johnson & Johnson that millions of doses of COVID vaccine produced at a troubled plant can’t be used because of possible contamination issues.
In a statement, the FDA said “several” batches of vaccine manufactured at the Emergent BioSolutions facility in the city of Baltimore are not suitable for use. Each batch is known to correspond to several million doses. “These actions followed an extensive review of records, including the production history of the facility and the testing performed to evaluate the quality of the product,” said FDA scientist Peter Marks.
The FDA is still deciding whether to allow the factory to reopen. Sixty million AstraZeneca doses produced there and earmarked to be donated abroad are currently being inspected for quality before they can be shipped.
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