FDA recalls QC Quality Choice menthol cough drops due to quality concerns from a manufacturing inspection in August 2025. No specific safety risk is stated, but the product may not meet quality standards.
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.
The FDA has recalled QC Quality Choice menthol cough drops after finding quality issues during a manufacturing inspection in August 2025. This recall does not indicate a specific safety risk but addresses potential product quality problems.
The recall was initiated by the FDA following observations during an August 2025 inspection that may impact product quality. However, the recall does not specify a safety hazard or risk of injury.
Anyone who purchased QC Quality Choice menthol cough drops with the lot numbers listed in the recall notice. People using these products for cough relief may be affected.
Check for the product name 'QC Quality Choice Menthol Cough Drops', 30-count bag, with lot numbers 20240720 (expiring 07/20/2026) or 20240524 (expiring 05/24/2026).
Look for the lot numbers 20240720 or 20240524 on the packaging to confirm if the product is recalled.
The recall does not state any safety risk or injury mechanism. The FDA's concern is about product quality, not safety.
Check for the lot numbers 20240720 (expiring 07/20/2026) or 20240524 (expiring 05/24/2026) on the packaging.
The recall does not specify a remedy, so no action is required beyond checking the product details.
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-0469-2026 — Xiamen Kang Zhongyuan Xiamen Kang Zhongyuan Hello, I own a Xiamen Kang Zhongyuan that is covered by recall D-0469-2026 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.
