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OLAAX International recalls
FDA enforcement reports naming OLAAX International as the recalling firm.
Recall reports
1
Class I (serious)
1
Most recent report
Jun 19, 2013
All
1
Food
0
Drugs
1
Severity
All classes
Class I: serious
Class II: moderate
Class III: low
Date
Product
Reason
Class
Jun 19, 2013
MAXILOSS Weight Advanced, 225 mg proprietary blend of herbs, supplied in 36 count capsu…
Drug · OLAAX International
Marketed Without an Approved NDA/ANDA: product contains sibutramine, a previously approved FDA drug removed from the U.S. marketplace for safety reasons, making it an unapproved new drug.
Class I
