Overview of recall records associated with Bacai Inc. Dba Ky Duyen House, including dates, categories and classifications where available.
Classification mix: Class I: 1.
Marketed Without an Approved NDA/ANDA: Bacai, Inc. DBA Ky Duyen House is voluntarily recalling Lite Fit USA, lot 13165, due to undeclared sibutramine, making it an unapproved new drug.
This page summarizes recall records in which the official source identifies Bacai Inc. Dba Ky Duyen House 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.
