RecallHawk
Class I Recall

Kian Pee Wan Capsules, 30-count bottles

Buy-Herbal

Summary

The FDA issued a Class I for Kian Pee Wan Capsules, 30-count bottles by Buy-Herbal. Reason: Marketed Without an Approved NDA/ANDA: Product contains undeclared drug ingredients dexamethasone and cyproheptadine..

Details

Source

Drug Recall

External ID

D-0769-2026

Action Date

2026-08-19

Status

Ongoing

Category

drug

Product Description

Kian Pee Wan Capsules, 30-count bottles

Lot/Code Info: All lots within expiry.

Quantity Affected: 71 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.

Type: Voluntary: Firm initiated

Recall Initiated: 2026-03-21

Company

Buy-Herbal

Flushing, NY

Context & Analysis

This is a Class I recall. Class I recalls are the most serious — there is a reasonable probability that use of or exposure to the product will cause serious health consequences or death.

This was one of 28 drug recalls issued in the same week, part of 68 drug-related FDA actions this month.

Buy-Herbal has 2 FDA actions in our database, including 2 recalls.

Frequently Asked Questions

What is a Class I recall?

A Class I recall is the most serious type. The FDA has determined there is a reasonable probability that the product will cause serious adverse health consequences or death. Consumers should stop using the product immediately.

What should I do if I have this product?

Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (Buy-Herbal) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does Buy-Herbal have FDA actions?

Buy-Herbal has 2 FDA actions in our database, including 2 recalls and 0 device clearances.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "D-0769-2026" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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