Ultra Seal Multi-Symptom Cramp Relief Recall: Cgmp Deviations

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Recalling firmUltra Seal Corporation521 Main St, N/A · New Paltz, NY 12561-1609

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✎ GovInfoNow plain-language explainer

What happened, in plain English

Ultra Seal Corporation is recalling certain Multi-Symptom Cramp Relief tablets due to cGMP deviations. This means the product may not meet quality standards, though the specific risk is not detailed in the recall notice.

Why it’s dangerous

The product was manufactured with cGMP deviations, which are quality control issues that could affect the product's safety and effectiveness. However, the recall notice does not specify what these deviations mean for consumer safety.

Who’s affected

People who purchased the recalled Multi-Symptom Cramp Relief tablets from First Aid Direct in Mason, Ohio. Those with the specific lot numbers AK9453 (expiring Jan 2022) or AK9716 (expiring July 2022) are most at risk.

How to tell if you have this one

Check for the product name 'Multi-Symptom Cramp Relief' with 2 tablets, manufactured for First Aid Direct in Mason, Ohio. Look for lot numbers AK9453 (expiring Jan 2022) or AK9716 (expiring July 2022).

Brand
Ultra Seal Corporation
Category
Drug

Based on the official FDA remedy

What to do — step by step

Check Product Details
Identify the lot number and expiration date on the product packaging to determine if it is in the recalled batch.

✎ GovInfoNow

Questions people ask

Is there a remedy for this product?

The recall notice does not specify a remedy.

What are the specific lot numbers for this recall?

The recalled lot numbers are AK9453 (expiring Jan 2022) and AK9716 (expiring July 2022).

How can I tell if I have the recalled product?

Check for the product name 'Multi-Symptom Cramp Relief' with 2 tablets, manufactured for First Aid Direct in Mason, Ohio, and lot numbers AK9453 or AK9716.

Take action

Contact Ultra Seal Corporation

We’ve drafted a message you can send Ultra Seal Corporation to request your refund or repair — edit it as you like.

✉️ Open in email

Subject: Recall D-0481-2022 — Ultra Seal Corporation Ultra Seal Corporation

Hello,

I own a Ultra Seal Corporation that is covered by recall D-0481-2022 from Ultra Seal Corporation.

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-0481-2022 (January 24, 2022) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-0481-2022 to see it in context.
Plain-language summary written by qwen3:4b on August 18, 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.

Ultra Seal Corporation recalls Multi-Symptom Cramp Relief (acetaminophen 325mg and Pamabrom 25mg), 2- tablet packets, Mfd. for First Aid Direct,

Recall notice