Overview of recall records associated with AA PRODUCTS Inc., including dates, categories and classifications where available.
Classification mix: Class II: 1.
CGMP Deviations: product manufactured at the same facility that produced product that FDA sampled and found to be subpotent for ethanol and contained methanol.
This page summarizes recall records in which the official source identifies AA PRODUCTS Inc. as the recalling firm or manufacturer. The number of records should not be treated as a safety rating or a measure of company size, because recall counts depend on product mix, reporting periods and how government records are organized.
Compare the dates, categories and classifications together rather than relying on the total alone. Open an individual record for the recalled product, reason, distribution details and current instructions available from the source.
