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Recall data is sourced from official U.S. government agencies (CPSC, FDA, NHTSA, USDA) and processed using AI to improve readability. This site is not affiliated with or endorsed by any government agency. Always refer to the original agency notice for authoritative information.

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Critical RiskFDA Drug

Blue Square Market, Inc.: Marketed Without An Approved NDA/ANDA: presence of undeclared Sibutramine and Phenolphthalein.; Marketed Without An Approved NDA/ANDA: presence of undeclared Sulfoaildenafil.

Agency Publication Date: November 17, 2015
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Affected Products

Product: LiDa DAIDAIHUA (also packaged as LiDa DAIDAIHUAJIAONANG), capsules, packaged in 1.6oz box 30 capsules per box, Kunming Dali Industry & Trade Co., Ltd

all lots

Product: KABOOM action strips, Sexual Performance Strips, packaged in 6.4oz box 12 strips per box, Nutrology USA LLC

all lots

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 71912
Status: Resolved
Manufacturer: Blue Square Market, Inc.
Manufactured In: United States
Units Affected: 2 products (25 boxes; 132 boxes)

Were You Affected by This Recall?

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AI-Enhanced Content: The summary, action steps, and risk assessment on this page were generated by AI from official government recall data to improve readability. This is not legal or medical advice. Always refer to the official agency sources below for authoritative information.

Sources: FDA iRES · Raw API Response

openFDA Disclaimer: This recall information is sourced from the openFDA API. Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Refer to the openFDA terms of service for more information.