FDA-identified quality issue with QC Quality Choice cherry cough drops from Xiamen Kang Zhongyuan. Recalled due to potential product quality concerns from August 2025 inspection.
This recall is being initiated following FDA's recommendation based on certain observations noted during an August 15, 2025, inspection of the manufacturing facility that may bear on product quality.
Xiamen Kang Zhongyuan Biotechnology Co., Ltd. is recalling QC Quality Choice cherry cough drops due to FDA-identified quality concerns from an August 2025 facility inspection. This recall affects products with specific lot numbers and expiration dates.
The recall was initiated by the FDA following observations during an August 15, 2025 inspection of the manufacturing facility that may impact product quality. The specific quality concern does not indicate immediate safety risks but requires attention due to regulatory findings.
Owners of QC Quality Choice cherry cough drops with lot numbers 20240524 (expiring May 2026) or 20240720 (expiring July 2026) are affected. Children and adults who use these products are at risk of potential quality issues.
Check for lot numbers 20240524 (expiring May 2026) or 20240720 (expiring July 2026) on the packaging. Products distributed by CDMA, Inc. in Novi, MI with NDC 83698-616-25 and UPC 635515993372 are included.
Look for lot numbers 20240524 (expiring May 2026) or 20240720 (expiring July 2026) on the packaging.
The FDA identified potential quality concerns during an August 15, 2025 inspection of the manufacturing facility.
Check the product for lot numbers 20240524 (expiring May 2026) or 20240720 (expiring July 2026). If you have these, contact the manufacturer for instructions.
The recall is due to potential quality issues, but no specific injury risk is mentioned in the official notice.
We’ve drafted a message you can send Xiamen Kang Zhongyuan to request your refund or repair — edit it as you like.
Subject: Recall D-0465-2026 — Xiamen Kang Zhongyuan Xiamen Kang Zhongyuan Hello, I own a Xiamen Kang Zhongyuan that is covered by recall D-0465-2026 from Xiamen Kang Zhongyuan. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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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.
