Quick Facts at a Glance
- Recall Date
- March 16, 2026
- Hazard Level
- HIGH
- Brands
- MECLIZINE HYDROCHLORIDE, American Health Packaging
- Category
- Health & Personal Care
- Sold At
- Multiple Retailers
- Geographic Scope
- 1 states
- At-Risk Groups
- GENERAL
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
- MECLIZINE HYDROCHLORIDE, American Health Packaging
- Product type
- Meclizine Hydrochloride Tablets 12.5 mg
- Model numbers
- Lot #1024852, Exp 9/30/2026
- UPC codes
- 60687-730, 60687-775, 60687-775-11, 60687-775-01, 60687-775-65, 60687-730-11, 60687-730-01, 60687-730-65
- Sold at
- Multiple Retailers
- Where affected
- ALL
Recall Timeline
Key dates and source checks for this recall record.
Recall announced
March 16, 2026
Reported by FDA DRUG
April 1, 2026
RecallRadar source check
April 8, 2026
Consumer action
Use the official remedy and keep documentation.
Hazard Information
Failed tablet specifications.
What You Should Do
Consumers and healthcare providers should stop using this product immediately. Contact Amerisource Health Services LLC or your healthcare provider for guidance. Notification method: Letter
About This Product
Meclizine is used to prevent and treat nausea, vomiting, and motion sickness. The 12.5 mg tablet is a common dose for adults for short-term relief.
Why This Is Dangerous
A failure to meet tablet specifications can lead to incorrect dosage, which may affect safety and efficacy.
Industry Context
This recall is not described as part of a broader industry pattern in the provided data.
Real-World Impact
Consumers with the affected lots may face dosing uncertainty. The recall is active and distributed nationwide.
Practical Guidance
How to identify if yours is affected
- Review NDC numbers on the bottle: 60687-775-65 and 60687-775-11.
- Check lot number 1024852 and expiration date 9/30/2026.
- Verify distributor: Amerisource Health Services LLC.
Where to find product info
FDA enforcement page and recall notice linked to the NDCs and lot numbers.
What timeline to expect
Recall notice indicates a letter will be issued with next steps. Specific refund timelines are not provided.
If the manufacturer is unresponsive
- File a consumer complaint with the FDA if the sponsor is unresponsive.
- Consult your pharmacist or healthcare provider for guidance.
How to prevent similar issues
- Check NDCs and lot numbers before purchasing medications.
- Buy from reputable pharmacies and verify packaging integrity.
- Keep all recall notices for reference.
Documentation advice
Keep the recall letter, packaging, and any correspondence with the pharmacy or provider. Photograph the product and packaging for records.
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Product Details
NDC 60687-775-65: 50 Tablets per carton [5 x 10], Rx Only, 697 cartons distributed nationwide in the U.S. NDC 60687-775-11: 12.5 mg Individual Dose, Rx Only, 697 cartons distributed nationwide. Distributor: Amerisource Health Services LLC, Columbus, OH 43217. Recall date: 2026-03-16. Status: Active. Manufactured by Meclizine Hydrochloride supplier. The package form includes both multi-dose cartons and single-dose units.
Reported Incidents
No injuries or incidents have been reported.
Key Facts
- 697 cartons recalled nationwide
- Distributor: Amerisource Health Services LLC
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Safety Guide
Not sure what to do next? Our guide walks you through the process step by step.
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