PEPTIME Energy Caffeine Tablets Recall: Cgmp Deviations

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Contact the company & request your remedy

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

No email on file — write to the address above instead.

✎ GovInfoNow plain-language explainer

What happened, in plain English

Ultra Seal Corporation is recalling PEPTIME Energy caffeine tablets (300mg) in 6-count packets and 100-count bottles due to cGMP deviations. This means the tablets may not meet quality standards and could pose safety risks.

Why it’s dangerous

cGMP deviations refer to failures in manufacturing quality control processes. This could mean the tablets do not meet safety or quality standards, potentially leading to health risks if consumed.

Who’s affected

People who purchased PEPTIME Energy caffeine tablets from DMD Pharmaceuticals in Noblesville, Indiana, likely own the affected lots 19E030 (6-count) or 19E031 (100-count).

How to tell if you have this one

Check for PEPTIME Energy caffeine tablets (300mg) in 6-count packets or 100-count bottles with lot numbers 19E030 or 19E031. The product was marketed by DMD Pharmaceuticals in Noblesville, Indiana.

Brand
Ultra Seal
Category
Drug

Based on the official FDA remedy

What to do — step by step

Check Product Lot Number
Look for lot numbers 19E030 on 6-count packets or 19E031 on 100-count bottles.

✎ GovInfoNow

Questions people ask

Why is this product being recalled?

The product was recalled due to cGMP deviations, which are failures in manufacturing quality control processes.

What should I do if I have the recalled product?

The recall record does not specify a remedy, so no action is required beyond checking the lot number.

Are there any safety risks from this product?

The recall record does not describe specific safety risks, only that there were cGMP deviations.

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-0502-2022 — Ultra Seal Ultra Seal

Hello,

I own a Ultra Seal that is covered by recall D-0502-2022 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-0502-2022 (January 24, 2022) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-0502-2022 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 PEPTIME Energy (caffeine 300mg) tablets, packaged in a) 6 count packets and b) 100-count bottles, Marketed by: DMD

Recall notice