Super Herbs 350 Mg recall
SUPER HERBS 350 mg, 30 capsules per bottle.
Why was Super Herbs 350 Mg recalled?
Marketed without an approved NDA/ANDA - presence of undeclared sibutramine, desmethylsibutramine (an active metabolite of sibutramine) and/or phenolphthalein.
What should I do if I have this product?
Review the official FDA enforcement record for current instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
All lots
- Product
- SUPER HERBS 350 mg, 30 capsules per bottle.
- Recalling firm
- Super Herbs
- Quantity
- 9 bottles
- Distribution
- 9 consignees - only 9 bottles distributed
- Recall date
- June 1, 2016
- Classification
- Class I
- Status
- Terminated
- Agency
- FDA (drug)