Cross-contamination of products containing Klamath AFA have occurred in the past. From 2018 to 2020, the
Food and Drug Administration did three product recalls, all by the same original harvesting company. Each recall found higher levels of microcystin than suggested by the
WHO and
EPA provisional guidelines, which is less than 1
microgram per gram. These investigations led to Class 2 voluntary recalls of the affected products. The products were all linked to several batches of AFA harvested by the company between 2015 and 2017. From these recalls, the FDA started working with harvesting companies to outline new industry practices and testing procedures for harvesting AFA. These now include: • At the time of harvest, examining AFA at the harvesting site for contaminating cyanobacteria. • At the time of harvest, testing the water and AFA for microcystins. • After harvest, testing the AFA slurry for microcystins. • Before selling AFA products, testing each lot or batch for microcystins. • Using more than one test method to confirm results. • Using a test method that can detect multiple variant forms of microcystins. • Using certified testing laboratories and validated methods. • Providing a certificate of analysis to purchasers for each lot or batch sold. Since these guidelines were developed, no product recalls have occurred. As of 2024, the FDA states that wild-harvested cyanobacteria is safe to eat. == See also ==