QC Quality Choice, Menthol-Cough Suppressant Oral Anesthetic, Cough Drops, Sugar Free, Honey Lemon Flavor, 25-count bag,
Summary
The FDA issued a Class II for QC Quality Choice, Menthol-Cough Suppressant Oral Anesthetic, Cough Drops, Sugar by Xiamen Kang Zhongyuan Biotechnology Co., Ltd.. Reason: This recall is being initiated following FDA's recommendation based on certain observations noted during an August 15, 2025, inspection of the manufac.
Details
Source
Drug Recall
External ID
D-0466-2026
Action Date
2026-04-22
Status
Ongoing
Category
drug
Product Description
QC Quality Choice, Menthol-Cough Suppressant Oral Anesthetic, Cough Drops, Sugar Free, Honey Lemon Flavor, 25-count bag, Distributed By: CDMA, Inc., Novi, MI 48375, Made in China, NDC: 83698-616-25, UPC: 635515993372.
Lot/Code Info: Lot # 20240720, Exp Date: 07/20/2026, Lot # 20241030, Exp Date: 10/30/2026.
Quantity Affected: N/A
Reason for Recall
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.
Distribution
US Nationwide.
Type: Voluntary: Firm initiated
Recall Initiated: 2026-03-20
Company
Context & Analysis
This is a Class II recall. Class II recalls indicate that use of or exposure to the product may cause temporary or medically reversible health consequences, or that the probability of serious consequences is remote.
This was one of 94 drug recalls issued in the same week, part of 267 drug-related FDA actions this month.
Xiamen Kang Zhongyuan Biotechnology Co., Ltd. has 15 FDA actions in our database, including 15 recalls.
Frequently Asked Questions
What is a Class II recall?
A Class II recall means the product may cause temporary or medically reversible adverse health consequences, or the probability of serious adverse consequences is remote. Consumers should discontinue use.
What should I do if I have this product?
Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (Xiamen Kang Zhongyuan Biotechnology Co., Ltd.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Xiamen Kang Zhongyuan Biotechnology Co., Ltd. have FDA actions?
Xiamen Kang Zhongyuan Biotechnology Co., Ltd. has 15 FDA actions in our database, including 15 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "D-0466-2026" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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