Ultra Seal Corporation recalls 100-count PEPTIME Energy caffeine tablets due to cGMP deviations. Consumers should check lot numbers 19E021 and 19E022 for affected products.
cGMP deviations
Ultra Seal Corporation is recalling 100-count PEPT: Energy caffeine tablets because of manufacturing quality control issues. This recall affects products with lot numbers 19E021 and 19E022, which were sold by DMD Pharmaceuticals.
The recall is due to cGMP deviations, which means the manufacturing process did not meet quality standards. This could lead to inconsistent caffeine content or other safety issues in the product.
People who own or use PEPTIME Energy caffeine tablets with lot numbers 19E021 or 19E022 are affected. Those who consume these products are at risk due to potential quality control issues.
Check the lot number on the product label, which should be 19E021 or 19E022 for affected items. The product is a 100-count bottle of PEPTIME Energy caffeine tablets.
Look for lot numbers 19E021 or 19E022 on the product label to identify affected items.
Ultra Seal Corporation is recalling 100-count PEPTIME Energy caffeine tablets with lot numbers 19E021 and 19E022 due to cGMP deviations.
Check the lot number on the product label; affected items have lot numbers 19E021 or 19E022.
The recall does not specify a remedy, so contact Ultra Seal Corporation for further instructions.
We’ve drafted a message you can send Ultra Seal to request your refund or repair — edit it as you like.
Subject: Recall D-0501-2022 — Ultra Seal Ultra Seal Hello, I own a Ultra Seal that is covered by recall D-0501-2022 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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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.
