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FDA source record Class II Terminated

Notoginseng Formula Special Gout Granule; 100% Natural; 8 G x 10 PACKS; CITI TRADE INT'L LIMITED; ADDRESS: 3/FINTERNATIONAL PLAZA 20 SHEUNG YUET RD, KOWLOON BAY, KOWLOON; "Nouri...

Recall Date: 2024-01-14 Recalling Firm: 8TH AVE PHARMACY Record Ref: F-0810-2024

FINDARECALL QUICK READ

What this record tells you

This FDA record concerns Notoginseng Formula Special Gout Granule; 100% Natural; 8 G x 10 PACKS; CITI TRADE INT'L LIMITED; ADDRESS: 3/FINTERNATIONAL PLAZA 20 SHEUNG YUET RD, KOWLOON BAY, KOWLOON; "Nouri... and names 8TH AVE PHARMACY as the recalling firm. Use the source fields below to narrow the match, then verify the exact item and current remedy on the issuing-agency page.

  • Firm: 8TH AVE PHARMACY
  • Classification: Class II
  • Status: Terminated
  • Recall date: 2024-01-14
Best identifiers to check for a FDA record

Compare UPC/GTIN, lot or batch code, package size, flavor or variety, and any best-by/use-by date listed in the notice.

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Product Description & Identification

Notoginseng Formula Special Gout Granule; 100% Natural; 8 G x 10 PACKS; CITI TRADE INT'L LIMITED; ADDRESS: 3/FINTERNATIONAL PLAZA 20 SHEUNG YUET RD, KOWLOON BAY, KOWLOON; "Nourish and helps the kidney with detoxification. Effectively dissolves uric acid crystals in joints. Has a curative effect on a variety of inflammatory symptoms caused by gout and high levels of uric acid, including pain and swollen joints."

Reason for Recall / Hazard Identified

Product contains undeclared Diclofenac and Dexamethasone Acetate

How to Check Whether Your Product Matches

A matching product name or photograph is not enough by itself. Compare every identifier available on your item or packaging with the official notice.

  1. Confirm the full product and brand or recalling-firm name.
  2. Compare package size, color, flavor, model, style, or configuration when listed.
  3. Check UPC, lot, batch, serial, date code, recall number, or USDA establishment number.
  4. Review the recall date and distribution information without assuming every seller is listed.
  5. Open the official FDA source below and follow its current instructions.

If a required identifier is missing, contact the recalling company or issuing agency through the official notice rather than guessing.

Consumer Action Recorded in the Source

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Distribution & Affected States

AL,CO,FL,GA,HI,IL,IN,LA,MD,MI,MN,MO,MS,NC,NJ,NV,OH,OR,PA,TN,TX,UT,VA,WA,WI

Verify With the Issuing Agency

This record was last updated in our index on 2026-08-09 21:59:13 UTC. Because recall enforcement statuses and instructions evolve, always verify details directly with the issuing government agency.

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Record Transparency

Issuing agency
FDA
Source ID
F-0810-2024
Indexed update
2026-08-09 21:59:13 UTC
Official source
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