# FDA recall D-0909-2016

> **Super Herbs** · Class I · drug recall initiated 2015-11-23.

## Product

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.

## Distribution

9 consignees - only 9 bottles distributed

## Key facts

- **Recall number:** D-0909-2016
- **Recalling firm:** Super Herbs
- **Classification:** Class I
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2015-11-23
- **Report date:** 2016-06-01
- **Termination date:** 2024-10-01

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Miami, FL, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-0909-2016

## Citation

> AI Analytics. FDA recall D-0909-2016. Retrieved 2026-05-26 from https://api.ai-analytics.org/recall/D-0909-2016. Source: US FDA. Licensed CC0.

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