# FDA recall D-0769-2026

> **Buy-Herbal** · Class I · drug recall initiated 2026-03-21.

## Product

Kian Pee Wan Capsules, 30-count bottles

## Reason for recall

Marketed Without an Approved NDA/ANDA: Product contains undeclared drug ingredients dexamethasone and cyproheptadine.

## Distribution

Product was sold to individual consumers via ebay third party seller.

## Key facts

- **Recall number:** D-0769-2026
- **Recalling firm:** Buy-Herbal
- **Classification:** Class I
- **Product type:** drug
- **Status:** Ongoing
- **Initiation date:** 2026-03-21
- **Report date:** 2026-08-19

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Flushing, NY, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-0769-2026

## Citation

> AI Analytics. FDA recall D-0769-2026. Retrieved 2026-09-01 from https://api.ai-analytics.org/recall/D-0769-2026. Source: US FDA. Licensed CC0.

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*[Dataset catalog](/datasets/) · [FDA recalls dataset](/datasets/fda-recalls) · CC0 1.0*
