United Pacific Zhong Hua Jiu Menthol Patch Recall: Substandard Manufacturing
United Pacific recalls Zhong Hua Jiu menthol 1% patches due to substandard manufacturing processes. Affected lots have specific expiration dates and UPC/NDC codes.
Recall notice
CGMP Deviations: the product was produced with substandard GMP manufacturing processes.
Contact the company
What happened, in plain English
United Pacific is recalling Zhong Hua Jiu menthol 1% patches produced with substandard manufacturing processes. This recall is due to potential quality issues that could affect product safety. Read more at govinfonow.com/recall/40712-united-pacific-zhong-hua-jiu-menthol-patch-recall-substandard-manufacturing.
Source Summary by GovInfoNow · govinfonow.com/recall/40712-united-pacific-zhong-hua-jiu-menthol-patch-recall-substandard-manufacturing · Updated October 7, 2026 · FDA enforcement record: FDA #D-0624-2018
Cite this page
“United Pacific Zhong Hua Jiu Menthol Patch Recall: Substandard Manufacturing.” GovInfoNow, updated October 7, 2026. https://govinfonow.com/recall/40712-united-pacific-zhong-hua-jiu-menthol-patch-recall-substandard-manufacturing. Based on FDA recall #D-0624-2018 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0624-2018%22&limit=1).
Why it’s dangerous
The patches were made using manufacturing processes that did not meet current Good Manufacturing Practices (CGMP). This could lead to inconsistent quality and potential safety issues with the product.
Who’s affected
People who own or use Zhong Hua Jiu menthol 1% patches with the specified UPC and NDC codes are affected. Those who have the patches from the listed production lots are at risk.
How to tell if you have this one
Check for the UPC 6 924938 100226 and NDC 53614-001-02 on the packaging. The product may have specific lot numbers and expiration dates listed in the recall notice.
- Brand
United Pacific- Product
Zhong Hua Jiu (menthol 1%) Patch, Distributed by United Pacific Company, UPC 6 924938 100226, NDC 53614-001-02- Category
Drug
What to do — step by step
Check Product Details
Look for the UPC 6 924938 100226 and NDC 53614-001-02 on the packaging to confirm if the product is affected.
Where it went and when
Where it was distributed
Distributed nationwide.
FDA distribution: “Nationwide within US” States read from FDA’s own wording; “not listed” means the notice does not name it.
Distributed nationwide.
Recall timeline
FDA terminated this recall 10 months after the firm started it.
- Firm started the recall
- FDA classified it Class II
- Published in FDA’s Enforcement Report
- FDA terminated the recall
Dates from the agency record only; steps without a date are left out.
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Where this comes from
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
- Official source: FDA Recall #D-0624-2018 (March 29, 2018) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-0624-2018 to see it in context.
- Plain-language summary written by qwen3:4b on October 7, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
- GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.