Bee Xtreme Recalls

Overview of recall records associated with Bee Xtreme, including dates, categories and classifications where available.

3recall records

Oct 19, 2016latest record date

Oct 19, 2016earliest record date

Recall history in this database

Classification mix: Class I: 3.

DrugOct 19, 2016

Bee Xtreme Oasis Dietary Supplement Capsules, 500 mg, 45 count bottles recall — FDA D-0020-2017

Marketed without an Approved NDA/ANDA; FDA analysis found them to contain sibutramine and phenolphthalein

Class IFDA: TerminatedBee Xtreme

DrugOct 19, 2016

Bee Xtreme Jenesis Dietary Supplement Capsules, 350 mg, 60 count bottles recall — FDA D-0021-2017

Marketed without an Approved NDA/ANDA; FDA analysis found them to contain sibutramine and phenolphthalein

Class IFDA: TerminatedBee Xtreme

DrugOct 19, 2016

Bee Xtreme La' Trim Plus Dietary Supplement Capsules, 350 mg, 60 count bottles recall — FDA D-0019-2017

Marketed without an Approved NDA/ANDA; FDA analysis found them to contain sibutramine and phenolphthalein

Class IFDA: TerminatedBee Xtreme

Understanding this recall history

This page summarizes recall records in which the official source identifies Bee Xtreme 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.