FDA Class II Recall: QUALITY CHOICE by Xiamen Kang Zhongyuan Biotechnology Co., Ltd. — Recall Details

Key facts

What consumers should do

Because this recall carries FDA's middle severity classification, anyone who has this product should stop using it and follow the recalling firm's instructions, even though serious harm is considered unlikely for this classification. Specifically, check whether the product in your possession matches the description on file with FDA -- QC Quality Choice, Menthol-Cough Suppressant Oral Anesthetic, Cough Drops, Honey Lemon Flavor, 30-count bag, Distributed By: CDMA Inc., Novi, MI 48375, Made in China, NDC: 83698-617-30, UPC: 63551598673. -- and the recall number D-0468-2026. If it matches, stop using or distributing it and contact Xiamen Kang Zhongyuan Biotechnology Co., Ltd. or the point of purchase for return or replacement instructions. Retailers and distributors holding affected inventory should quarantine it and follow the firm's written recall notice.

What this classification means

FDA classifies a recall as Class II when using the recalled product, or being exposed to it, may cause temporary or medically reversible adverse health consequences, or when the probability of serious adverse health consequences is remote. In this case, the recalling firm is Xiamen Kang Zhongyuan Biotechnology Co., Ltd. and the affected product is described in FDA's record as: QC Quality Choice, Menthol-Cough Suppressant Oral Anesthetic, Cough Drops, Honey Lemon Flavor, 30-count bag, Distributed By: CDMA Inc., Novi, MI 48375, Made in China, NDC: 83698-617-30, UPC: 63551598673.. FDA's stated reason for the recall is: 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 recall is tracked under FDA recall number D-0468-2026 and carries a status of Ongoing as of the most recent FDA enforcement report. This classification reflects FDA's assessment of the product defect described above, not a prediction about any specific patient outcome. FDA maintains a public enforcement report database so that consumers, physicians, and purchasers can look up the exact product identifiers involved before deciding what to do. Recall status can change while FDA and the recalling firm continue corrective actions, so checking the firm's own notice for the most current guidance is recommended.

Xiamen Kang Zhongyuan Biotechnology Co., Ltd.’s FDA history

Argus HQ has recorded 15 total FDA actions tied to Xiamen Kang Zhongyuan Biotechnology Co., Ltd.: 0 warning letters, 15 recalls, 0 approval records, and 0 Form 483 inspection citations.

Frequently asked questions

What should someone who has this product do?

Because this recall carries FDA's middle severity classification, anyone who has this product should stop using it and follow the recalling firm's instructions, even though serious harm is considered unlikely for this classification. Check the product against FDA's description (QC Quality Choice, Menthol-Cough Suppressant Oral Anesthetic, Cough Drops, Honey Lemon Flavor, 30-count bag, Distributed By: CDMA Inc., Novi, MI 48375, Made in China, NDC: 83698-617-30, UPC: 63551598673.) and recall number D-0468-2026, then follow Xiamen Kang Zhongyuan Biotechnology Co., Ltd.'s recall instructions.

Has Xiamen Kang Zhongyuan Biotechnology Co., Ltd. had other FDA recalls or enforcement actions?

Yes. Argus HQ has recorded 15 total FDA actions tied to Xiamen Kang Zhongyuan Biotechnology Co., Ltd., including 15 recalls and 0 warning letters.

What is the FDA recall number for this event?

FDA recall number D-0468-2026.

What is the current status of this recall?

Status as recorded by FDA: Ongoing.

Related enforcement actions