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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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Medium RiskFDA Drug
Medications & Supplements/Topical Products

United Pacific Co Ltd: Zhong Hua Jiu Menthol Patches Recalled for Substandard Manufacturing

Agency Publication Date: April 10, 2018
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Summary

United Pacific Co Ltd is recalling approximately 15,190 boxes of Zhong Hua Jiu (menthol 1%) Patches because they were produced using substandard manufacturing processes that do not meet safety and quality standards. These topical pain relief patches were distributed nationwide in the United States. Consumers who have these products should immediately stop using them and contact their healthcare provider or pharmacist for guidance.

Risk

The product was manufactured with deviations from Current Good Manufacturing Practice (CGMP) regulations, meaning the quality, safety, and effectiveness of the patches cannot be guaranteed. Substandard manufacturing processes can lead to contamination or incorrect levels of active ingredients, potentially causing skin irritation or failing to treat pain effectively.

What You Should Do

  1. Check your medicine cabinet for 'Zhong Hua Jiu (menthol 1%) Patch' boxes with UPC code 6 924938 100226 and NDC 53614-001-02.
  2. Identify if you have any of the following affected lot numbers and expiration dates: Lot 14122921 (Exp. 12/30/2019), Lot 15091512 (Exp. 9/15/2020), Lot 6032321 (Exp. 3/23/2021), or Lot 17030921 (Exp. 3/09/2022).
  3. Stop using the patches immediately if they match the affected lot numbers.
  4. Contact your healthcare provider or pharmacist for guidance regarding the use of this product and to discuss alternative treatments.
  5. Return any unused product to the place of purchase for a refund and contact United Pacific Company at their South El Monte, California location for further instructions.
  6. For additional questions, contact the FDA Consumer Complaint hotline at 1-888-723-3332 (1-888-SAFEFDA) or visit www.fda.gov/safety/recalls.

Your Remedy Options

💰Full Refund
How to: Contact your healthcare provider or pharmacist for guidance. Return any unused product to the pharmacy for a refund

Affected Products

Product: Zhong Hua Jiu (menthol 1%) Patch
Model:
NDC 53614-001-02
UPC Codes:
6924938100226
Lot Numbers:
14122921 (Exp. 12/30/2019)
15091512 (Exp. 9/15/2020)
6032321 (Exp. 3/23/2021)
17030921 (Exp. 3/09/2022)
Date Ranges: Expiration 12/30/2019, Expiration 9/15/2020, Expiration 3/23/2021, Expiration 3/09/2022

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 79693
Status: Resolved
Manufacturer: United Pacific Co Ltd
Manufactured In: United States
Units Affected: 15,190 boxes
Distributed To: Nationwide

Were You Affected by This Recall?

If you or a family member were harmed by this recalled product, you may have legal rights. Consider consulting a consumer protection attorney to understand your options for compensation.

Find an Attorney

This is general information, not legal advice. Go Backs is not a law firm and does not provide legal services.

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.