FDA-identified quality issue with QC Quality Choice throat soothing drops from Xiamen Kang Zhongyuan Biotechnology. Recall covers specific lot numbers and distribution dates. Consumers should check product details and follow official instructions.
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 is recalling QC Quality Choice throat soothing drops due to a quality concern identified during an FDA inspection. This recall affects specific lot numbers and distribution dates, but does not indicate a safety risk to consumers.
The FDA identified potential quality issues during an August 15, 2025 inspection of the manufacturing facility. This could affect product safety or effectiveness, but the recall does not indicate a risk of injury or serious harm.
Consumers who purchased QC Quality Choice throat soothing drops with lot number 20240720 and expiration date 07/20/2026 are affected. Those using the product for throat relief may be at risk of quality issues.
Check for the product name 'QC Quality Choice, Pectin Oral Demulcent, Throat Soothing Drops, Creamy Strawberry Flavor' with a 30-count bag. Look for lot number 20240720 and expiration date 07/20/2026.
Verify the product name, lot number, and expiration date to confirm if it is part of this recall.
The recall is due to a quality concern identified by the FDA, not a safety risk. The product does not pose a risk of injury or serious harm.
Check the product details to see if it matches the recall criteria. If it does, contact the manufacturer for further instructions.
Look for the lot number 20240720 and expiration date 07/20/2026 on the product label.
We’ve drafted a message you can send Xiamen Kang Zhongyuan Biotechnology to request your refund or repair — edit it as you like.
Subject: Recall D-0467-2026 — Xiamen Kang Zhongyuan Biotechnology Xiamen Kang Zhongyuan Biotechnology Hello, I own a Xiamen Kang Zhongyuan Biotechnology that is covered by recall D-0467-2026 from Xiamen Kang Zhongyuan Biotechnology. 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.
