Ultra Seal Electrolyte Tablets Recall: Cgmp Deviations in Supplements

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Contact the company & request your remedy

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 2-count electrolyte supplement tablets that were manufactured with cGMP deviations. This means the product may not meet quality standards, though serious injury risks are not specified in the recall.

Why it’s dangerous

The product was made with cGMP deviations, which are quality control failures in manufacturing. This could mean the tablets do not meet the required safety and purity standards, but the recall does not specify a risk of serious injury or illness.

Who’s affected

People who purchased the 2-count electrolyte tablets from Honeywell Safety Products USA in Smithfield, RI, with lot numbers AK9797 or AK9254. Those using these supplements for medical purposes may be at slightly higher risk due to potential quality issues.

How to tell if you have this one

Check for the product name 'Electrolyte Supplement Tablets' with 2-count packets. Look for lot numbers AK9797 or AK9254 on the packaging. The product was distributed by Honeywell Safety Products USA in Smithfield, RI.

Brand
Ultra Seal
Category
Drug

Based on the official FDA remedy

What to do — step by step

Check Product Details
Look for lot numbers AK9797 or AK9254 on the packaging to confirm if the product is affected.

✎ GovInfoNow

Questions people ask

Is there a risk of serious injury from these tablets?

The recall mentions cGMP deviations but does not specify any risk of serious injury or illness.

How can I get a refund or replacement?

The recall does not mention any remedy or action for refunds or replacements.

Which lot numbers are affected?

Lot numbers AK9797 and AK9254 from Honeywell Safety Products USA in Smithfield, RI.

Take action

Contact Ultra Seal

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

✉️ Open in email

Subject: Recall D-0515-2022 — Ultra Seal Ultra Seal

Hello,

I own a Ultra Seal that is covered by recall D-0515-2022 from Ultra Seal.

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-0515-2022 (January 24, 2022) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-0515-2022 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 ELECTROLYTE Supplement Tablets (calcium 5.2 mg, Potassium 20.8 mg, Magnesium 6 mg ) 2-count packets, Dist. by Honeywell

Lower-risk recall