Quick Facts at a Glance
- Recall Date
- March 20, 2026
- Hazard Level
- HIGH
- Brands
- DISCOUNT DRUG MART, Xiamen Kang Zhongyuan Biotechnology Co., Ltd.
- Geographic Scope
- 1 states
What to Do Now
Use this page like a recall checklist: verify the product first, then act on the official remedy.
Immediate steps
- 1Stop using the product until you confirm whether it is included in the recall.
- 2Compare the product label, model number, UPC, color, size, and purchase location against the identifiers below.
- 3Follow the official remedy from FDA - Drug Safety; save photos, receipts, labels, and correspondence before contacting the company.
- 4If the product could harm a child, older adult, pet, or patient, move it out of reach immediately.
Check these identifiers
- Brand
- DISCOUNT DRUG MART, Xiamen Kang Zhongyuan Biotechnology Co., Ltd.
- Model numbers
- Lot # 20241030, Exp Date: 10/30/2026
- UPC codes
- 83698-102, 83698-102-30, 0933510370
- Where affected
- ALL
Recall Timeline
Key dates and source checks for this recall record.
Recall announced
March 20, 2026
Reported by FDA DRUG
April 22, 2026
RecallRadar source check
April 29, 2026
Consumer action
Use the official remedy and keep documentation.
Hazard Information
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.
What You Should Do
Consumers and healthcare providers should stop using this product immediately. Contact Xiamen Kang Zhongyuan Biotechnology Co., Ltd. or your healthcare provider for guidance. Notification method: Letter
Get instant alerts for DISCOUNT DRUG MART recalls
Be the first to know. Free instant alerts to your inbox.
Full Description
Discount Drug Mart Food Market, Cough Drops, Menthol -Cough Suppressant Anesthetic, 30-count bag, Distributed By: Drug Mart-Food Fair, Medina, Ohio 44256, Made in China, NDC: 83698-102-30, UPC: 093351037085.. Generic: COUGH DROPS MENTHOL; Brand: DISCOUNT DRUG MART. Reason: 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.. Classification: Class II. Quantity: N/A. Distribution: US Nationwide.
Browse More Recalls
Safety Guide
Not sure what to do next? Our guide walks you through the process step by step.
Read: How to Get Refunds and ReplacementsWant to Know First?
Get instant alerts for recalls that affect you. Free forever.