With Listeria monocytogenes having been detected in product samples at a family sprout facility by the state department of agriculture in September 2024, and a recall initiated, the FDA inspected the facility in October. Noting violations of the Produce Safety Rule (21CFR 112), the agency issued a 483. No response was received so the FDA then issued a warning letter with concerns about the environmental monitoring program (EMP).
EMP issues included an insufficiency of sampling sites that would enable the presence of Listeria or L. monocytogenes. Additionally, when follow-up product testing was conducted by the state ag department in January 2025, L. monocytogenes was again detected, and another recall initiated. Additional comments from the FDA revealed insanitary food contact surfaces and significant rodent activity.
