Wilshire Pharmaceuticals Inc recalls Meclizine HCl Tablets, USP, 12.5 mg, 100 Tablets bottles, Rx Only, Mfd. for: Wilshire Pharmaceuticals, Inc., Atlanta,
Wilshire Pharmaceuticals recalls 12.5 mg Meclizine tablets due to failed dissolution specifications. This may affect medication effectiveness. Contact for return instructions.
Lower-risk recall
Failed Dissolution Specifications
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What happened, in plain English
Wilshire Pharmaceuticals is recalling 12.5 mg Meclizine HCl tablets that failed dissolution tests. This could mean the medication doesn't work as intended, so affected users should stop using them. Read more at govinfonow.com/recall/36531-wilshire-meclizine-tablets-recall-failed-dissolution-specifications.
Source Summary by GovInfoNow · govinfonow.com/recall/36531-wilshire-meclizine-tablets-recall-failed-dissolution-specifications · Updated October 4, 2026 · FDA enforcement record: FDA #D-0258-2021
Cite this page
“Wilshire Meclizine Tablets Recall: Failed Dissolution Specifications.” GovInfoNow, updated October 4, 2026. https://govinfonow.com/recall/36531-wilshire-meclizine-tablets-recall-failed-dissolution-specifications. Based on FDA recall #D-0258-2021 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0258-2021%22&limit=1).
Why it’s dangerous
The tablets failed dissolution specifications, meaning they may not dissolve properly in the body. This could lead to inconsistent medication levels and reduced effectiveness. The hazard is not life-threatening but affects how well the drug works.
Who’s affected
People who have the 12.5 mg Meclizine HCl tablets (100-count bottles) prescribed by a doctor. Those with specific medical conditions requiring this medication are most at risk.
How to tell if you have this one
Check for 12.5 mg Meclizine HCl tablets in 100-count bottles with NDC 52536-129-01. The lot number 18030318 was manufactured in Atlanta, GA, and expires March 2021.
- Brand
Wilshire Pharmaceuticals- Category
Drug
All 2 products in this recall
FDA lists each product line separately under one recall event. Check your product description, lot or code numbers against each row. Every row shares the hazard and remedy on this page.
- Classification
Class II- Status
Terminated- Distribution
FL, TX
| Recall number | Product, codes & lots | Quantity |
|---|---|---|
| D-0258-2021 | Meclizine HCl Tablets, USP, 12.5 mg, 100 Tablets bottles, Rx Only, Mfd. for: Wilshire Pharmaceuticals, Inc., Atlanta, GA 30328, Product of India, NDC 52536-129-01; Lot #: 18030318, Exp 03/2021 | 2112 bottles |
| D-0259-2021 | Meclizine HCl Tablets, USP, 25 mg, 100 Tablets bottles, Rx Only, Mfd. for: Wilshire Pharmaceuticals, Inc., Atlanta, GA 30328, Product of India, NDC 52536-133-01; Lot #: 18030329, 18030330, 18030331, Exp 03/2021. | 35928 bottles |
What to do — step by step
Stop Using Tablets
Discard the recalled Meclizine HCl tablets immediately as they may not work properly.
Questions people ask
Why is this product being recalled?
The tablets failed dissolution specifications, meaning they may not dissolve properly in the body and could be less effective.
How can I tell if I have the recalled product?
Look for 12.5 mg Meclizine HCl tablets in 100-count bottles with NDC 52536-129-01 and lot number 18030318.
What should I do if I have the recalled product?
Discard the tablets immediately as they may not work properly.
Contact Wilshire Pharmaceuticals
We’ve drafted a message you can send Wilshire Pharmaceuticals to request your refund or repair — edit it as you like.
Subject: Recall D-0258-2021 — Wilshire Pharmaceuticals Wilshire Pharmaceuticals Hello, I own a Wilshire Pharmaceuticals that is covered by recall D-0258-2021 from Wilshire Pharmaceuticals. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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Where this comes from
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
- Official source: FDA Recall #D-0258-2021 (February 4, 2021) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-0258-2021 to see it in context.
- Plain-language summary written by qwen3:4b on October 4, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
- GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.