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FDA pulls emergency authorization of J&J’s Covid-19 shot after final batch expired last month

“FDA has determined that it is appropriate to protect the public health or safety to revoke this authorization.”


The Food and Drug Administration (FDA) has pulled its emergency authorization for the Johnson & Johnson Covid-19 vaccine after the pharmaceutical giant’s Janssen unit made the request for removal.

Bloomberg reported that Janssen Pharmaceuticals, a company owned by Johnson & Johnson, told the FDA that previously acquired jabs have reached their expiration date and that US demand for the product is no more.

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