The U.S. Food and Drug Administration issued a warning letter to Optum Infusion Services over unsanitary conditions at one of its locations where it compounds drugs.
The FDA inspected an Optum Infusion facility in Chandler, Ariz., in March 2022 and found "serious deficiencies in your practices for producing drug products intended or expected to be sterile, which put patients at risk," the FDA wrote in the letter posted publicly on Tuesday.
Optum is owned by Minnetonka-based UnitedHealth Group, which ranks among the five largest public companies in the U.S. UnitedHealth Group CEO Andrew Witty was previously CEO of Eden Prairie-based Optum.
Because of the deficiencies found in the inspection, the drug products produced did not meet federal regulations, the FDA said.
"You did not perform adequate product evaluation and take appropriate corrective action after vermin was observed in your production area," the letter said. "Vermin are a source of microbial contamination."
The FDA sent the warning letter to Optum in mid-December.
In the letter, the FDA recommended several steps for Optum to address the concerns.
"FDA strongly recommends that your management undertake a comprehensive assessment of operations, including facility design, procedures, personnel, processes, maintenance, materials and systems," the letter said. "A third party consultant with relevant sterile drug processing expertise should assist you in conducting this comprehensive evaluation."