NewsBreak: FDA sends warning to American Cruise Lines after guests contract Legionnaires’ disease (Abomination Shot Adverse Events)

The Food and Drug Administration said American Cruise Lines had not provided sufficient proof of changes to procedures after multiple guests were diagnosed with Legionnaires’ disease, according to a warning letter to the line.

The agency found evidence of legionella bacteria, which causes the illness, in the potable water systems of the line’s American Star and American Heritage vessels after inspecting them periodically between December 2021 and August 2022, according to the Jan. 24 letter. The agency addressed the letter to the line’s executive vice president, Paul E. Taiclet

American Cruise Lines had not provided adequate documentation of new measures and verification of their effectiveness, according to the FDA. Any failure on the cruise line’s part to “adequately address this matter may result in legal action including, without limitation, seizure and injunction,” the letter said.

The cruise line “immediately responded with the documentation requested,” American Cruise Lines spokesperson Alexa Paolella told USA TODAY.

“More importantly, American took the matter very seriously in 2021, and implemented new water management policies and equipment on its ships,” Paolella said in an email. “We have had no further cases since 2021, nor any others in our company’s history.” The cruise line added that all potentially impacted guests were quickly notified.

A spokesperson for the FDA said in an email, “The FDA has received the firm’s response and will respond directly to the firm.”

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