FDA recall D-0769-2026

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

Status

Ongoing

Initiation date

2026-03-21

Report date

2026-08-19

Voluntary/Mandated

Voluntary: Firm initiated

Location

Flushing, NY, United States

Primary source

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