Quick Facts at a Glance
- Recall Date
- March 20, 2026
- Hazard Level
- HIGH
- Brands
- MGC HEALTH, 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
- MGC HEALTH, Xiamen Kang Zhongyuan Biotechnology Co., Ltd.
- Model numbers
- Lot# 20240524, Exp Date: 05/24/2026, Lot# 20240720, Exp Date: 07/20/2026, Lot# 20240730, Exp Date: 07/30/2026.
- UPC codes
- 83698-125, 83698-125-25, 83698-125-70, 3831730000
- 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
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Full Description
MGC Health, Menthol- Cough Suppressant, Oral Anesthetic, Cough Drops, Sugar Free, Honey Lemon, 25-count bag, Distributed By: Medical Group Care, LLC, 1035 Collier Center Way, STE 5, Naples, FL 34110, NDC: 83698-125-25, UPC: 383173000085. Generic: COUGH DROPS HONEY SUGAR-FREE; Brand: MGC HEALTH. 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.
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Safety Guide
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