Ultra Seal Corporation recalls DBI 357 Super Magnum Quick Energy Stimulant tablets due to cGMP deviations. Affected lots include 36-count, 100-count, and 500-count bottles with specific expiration dates.
cGMP deviations
Ultra Seal Corporation is recalling DBI 357 Super Magnum Quick Energy Stimulant tablets (caffeine 200mg) because of cGMP deviations. This means the product may not meet quality standards, though serious injury risks aren't specified in the recall.
The recall is due to cGMP (current Good Manufacturing Practice) deviations, which means the product may not meet quality standards. This could affect the safety and effectiveness of the caffeine tablets, though serious injury risks aren't explicitly stated in the recall.
People who purchased the DBI 357 Super Magnum Quick Energy Stimulant tablets in 36-count, 100-count, or 500-count bottles with specific lot numbers and expiration dates are affected. Those using the product for energy stimulation are most at risk due to potential quality issues.
Check for the product name 'DBI 357 Super Magnum Quick Energy Stimulant' in 36-count, 100-count, or 500-count bottles. Look for specific lot numbers and expiration dates listed in the recall notice.
Identify the lot number and expiration date on the packaging to determine if your product is affected.
The recall states there were cGMP deviations, but it does not specify that the product is unsafe or causes serious injury. The manufacturer recommends checking if your product is affected.
The recall does not provide a specific remedy, so you should check the product details to see if it is affected. If it is, contact the manufacturer for further instructions.
Yes, affected lots include specific numbers like C19065 (exp. 03/2022), F19081 (exp. 06/2022), and others with corresponding expiration dates.
We’ve drafted a message you can send DBI to request your refund or repair — edit it as you like.
Subject: Recall D-0472-2022 — DBI DBI Hello, I own a DBI that is covered by recall D-0472-2022 from DBI. 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.
