FDA-ordered recall of Honey Lemon Cough Drops due to potential quality issues found during facility inspection. Product may not meet safety standards. Consumers should check labels for NDC 83698-617-30.
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 Honey Lemon Cough Drops because FDA identified quality concerns during a manufacturing facility inspection. This recall does not involve a specific safety hazard but addresses potential product quality issues that could affect safety.
The FDA identified quality concerns during an August 15, 2025 inspection of the manufacturing facility. These concerns may affect product safety standards, but the recall does not specify a direct health risk or injury mechanism.
Anyone who purchased the Honey Lemon Cough Drops with NDC 83698-617-30 from CDMA Inc. in Novi, MI. Children and infants are at slightly higher risk due to the product's use as an oral anesthetic.
Check for the product name 'QC Quality Choice, Menthol-Cough Suppressant Oral Anesthetic, Cough Drops, Honey Lemon Flavor' on the label. Look for NDC code 83698-617-30 and expiration date 07/20/2026.
Look for the NDC code 83698-617-30 and expiration date 07/20/2026 on the packaging.
FDA identified quality concerns during an August 15, 2025 inspection of the manufacturing facility that may affect product safety standards.
The recall addresses potential quality issues but does not specify a direct health risk or injury mechanism.
Check for the NDC code 83698-617-30 and expiration date 07/20/2026 on the packaging.
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-0468-2026 — Xiamen Kang Zhongyuan Xiamen Kang Zhongyuan Hello, I own a Xiamen Kang Zhongyuan that is covered by recall D-0468-2026 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.
