FDA-ordered recall of Honey Lemon Cough Drops due to quality concerns from manufacturing inspection in August 2025. No specific safety risk described. Exchange program available.
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 Honey Lemon Cough Drops because of quality issues found during an FDA inspection in August 2025. This recall does not indicate a safety risk to consumers but follows FDA recommendations for product quality.
The recall was initiated by the FDA after observations during an August 15, 2025 inspection that may affect product quality. No specific safety hazard like injury or illness is described in the recall notice.
Anyone who purchased the Honey Lemon Cough Drops with NDC 83698-580-30, manufactured on Lot #20241030, expiring 10/30/2026. Military exchanges through Medical Group Care, LLC. are most likely affected.
Check for the NDC code 83698-580-30, Lot #20241030, and expiration date 10/30/2026 on the packaging. These cough drops were sold through military exchanges by Medical Group Care, LLC. in Naples, Florida.
Look for the NDC code 83698-580-30, Lot #20241030, and expiration date 10/30/2026 on the packaging.
The recall is for quality concerns, not safety risks. The FDA did not state that this product could cause injury or illness.
The recall notice does not specify a remedy, so no action is required beyond checking the product details.
The FDA recommended a recall after observations during an August 15, 2025 inspection that may affect product quality.
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-0456-2026 — Xiamen Kang Zhongyuan Xiamen Kang Zhongyuan Hello, I own a Xiamen Kang Zhongyuan that is covered by recall D-0456-2026 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.
