FDA-ordered recall of 30-count menthol cough drops due to quality concerns identified during August 2025 facility inspection. No specific safety risk described in recall notice.
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 30-count menthol cough drops after FDA identified potential quality issues during an August 2025 facility inspection. This recall does not indicate a specific safety hazard that could cause injury.
The recall was initiated by the FDA based on observations during an August 15, 2025 inspection of the manufacturing facility that may affect product quality. However, the recall notice does not specify what could go wrong with the product or any safety risks.
Owners of the 30-count menthol cough drops with lot number 20241030 and expiration date 10/30/2026 are affected. People using these cough drops for cough relief are most at risk if they have quality concerns.
Check for the 30-count bag labeled 'Menthol - Cough Suppressant Anesthetic' with lot number 20241030 and expiration date 10/30/2026. The product was distributed by Drug Mart-Food Fair in Medina, Ohio.
Verify the lot number (20241030) and expiration date (10/30/2026) on the packaging.
The FDA ordered this recall after identifying potential quality issues during an August 15, 2025 inspection of the manufacturing facility.
The recall notice does not describe any specific safety hazard that could cause injury.
Look for the 30-count bag with lot number 20241030 and expiration date 10/30/2026, distributed by Drug Mart-Food Fair in Medina, Ohio.
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-0460-2026 — Xiamen Kang Zhongyuan Xiamen Kang Zhongyuan Hello, I own a Xiamen Kang Zhongyuan that is covered by recall D-0460-2026 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.
