AllClear
PricingSign in
FDANovember 23, 2015drug

SUPER HERBS 350 mg, 30 capsules per bottle.

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

Marketed without an approved NDA/ANDA - presence of undeclared sibutramine, desmethylsibutramine (an active metabolite of sibutramine) and/or phenolphthalein.

What to do

FDA enforcement status: Terminated

Brands named

super herbssuper

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

Own something like this?

AllClear screens your whole list against every CPSC, FDA, USDA and NHTSA recall — and tells you the day a new one names something you own.

Start free — 200 items, no card →