SUPER HERBS 350 mg, 30 capsules per bottle.
Reported: June 1, 2016 Initiated: November 23, 2015 #D-0909-2016
Product Description
SUPER HERBS 350 mg, 30 capsules per bottle.
Reason for Recall
Marketed without an approved NDA/ANDA - presence of undeclared sibutramine, desmethylsibutramine (an active metabolite of sibutramine) and/or phenolphthalein.
Details
- Recalling Firm
- Super Herbs
- Units Affected
- 9 bottles
- Distribution
- 9 consignees - only 9 bottles distributed
- Location
- Miami, FL
Frequently Asked Questions
What product was recalled? ▼
SUPER HERBS 350 mg, 30 capsules per bottle.. Recalled by Super Herbs. Units affected: 9 bottles.
Why was this product recalled? ▼
Marketed without an approved NDA/ANDA - presence of undeclared sibutramine, desmethylsibutramine (an active metabolite of sibutramine) and/or phenolphthalein.
Which agency issued this recall? ▼
This recall was issued by the FDA Drug on June 1, 2016. Severity: Critical. Recall number: D-0909-2016.
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