The joint investigation report by the House select subcommittee on the coronavirus crisis and the Oversight and Reform Committee reinforced the negative portrait that emerged last year after the Food and Drug Administration suspended vaccine manufacturing at the plant.discovered
In a new finding in the subcommittee’s latest report, the panel report said employees removed yellow “hold tags” from two containers containing newly manufactured Johnson & Johnson vaccine one hour before FDA inspectors arrived at Emergent’s Bayview facility in Baltimore in February 2021 to conduct a site tour. The hold tags indicated a potential quality problem with the vaccine in the containers, the House panel found.
In another incident, the investigators reviewed an email from March 2021 in which an Emergent official told another executive to not disclose details of the contamination problems to the Biomedical Advanced Research and Development Authority, the federal government’s main pandemic contracting arm, after BARDA questioned the company about the unfolding crisis.
Out of 15 batches of the vaccine started between August 2021 and February 2022, six batches were either stopped before completion or rejected by Johnson & Johnson, the investigation found. The remaining nine batches were still being inspected and had not been cleared for distribution.It is not uncommon in vaccine manufacturing to have to stop production because the vaccine substance was out of specification, experts have told The Washington Post.
Kick their collective asses!
We done with covid.
Since when
Except J&J isn’t safe anyway. We’ve got bigger fish to fry.
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