“Public health and safety is a top priority and today’s action was a necessary step to ensure this company, which put patients unnecessarily at risk, does not operate within our state’s borders going forward,” Zoeller said in the release.
Zoeller said a license revocation means the company cannot operate in Indiana for at least seven years. The company could apply for a new license after that time, but the board would have to approve the license application.
In November, the Indiana Board of Pharmacy voted to indefinitely suspend the compounding pharmacy's non-resident pharmacy license and the Attorney General’s office recently filed a licensing complaint against the company. Zoeller said the pharmacy failed to ensure its epidural steroid injections were safe for patients, which led to devastating harm.
As of Feb. 4, the U.S. Centers for Disease Control and Prevention identified 10 deaths and 79 total cases of fungal meningitis in Indiana stemming from epidural steroid injections produced by the pharmacy. Nationwide, the outbreak involved 696 cases and 45 deaths across 20 states.