Overview of recall records associated with Hi Tech Pharmaceuticals, including dates, categories and classifications where available.
Classification mix: Class I: 14, Class II: 1.
The firm was notified by the FDA that the product contains the unapproved food additive 1,4-dimethylamylamine (DMAA).
During an inspection by the FDA the firm was notified by FDA that the product contains undeclared milk, wheat & soy.
During an inspection by the FDA the firm was notified by FDA that the product contains undeclared egg, milk, wheat & soy.
During an inspection by the FDA the firm was notified by FDA that the product contains undeclared milk, wheat & soy.
During an inspection by the FDA the firm was notified by FDA that the product contains undeclared milk, wheat & soy.
During an inspection by the FDA the firm was notified by FDA that the product contains undeclared milk, wheat & soy.
During an inspection by the FDA the firm was notified by FDA that the product contains undeclared milk, wheat & soy.
During an inspection by the FDA the firm was notified by FDA that the product contains undeclared milk, wheat & soy.
During an inspection by the FDA the firm was notified by FDA that the product contains contains wheat but the label states it is "Gluten Free".
During an inspection by the FDA the firm was notified by FDA that the product contains undeclared milk, wheat & soy.
During an inspection by the FDA the firm was notified by FDA that the product contains undeclared milk, wheat & soy.
During an inspection by the FDA the firm was notified by FDA that the product contains undeclared milk, wheat & soy.
During an inspection by the FDA the firm was notified by FDA that the product contains undeclared milk, wheat & soy.
During an inspection by the FDA the firm was notified by FDA that the product contains undeclared milk, wheat & soy.
During an inspection by the FDA the firm was notified by FDA that the product contains undeclared milk, wheat & soy.
This page summarizes recall records in which the official source identifies Hi Tech Pharmaceuticals 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.
