Ultra Seal Corporation recalls Cystex Urinary Pan Relief tablets due to cGMP deviations. Affected lots expire by 2022. Consumers should check packaging for lot numbers and expiration dates.
cGMP deviations
Ultra Seal Corporation is recalling Cystex Urinary Pan Relief tablets that were made with cGMP deviations. This means the product may not be safe for use as intended. Consumers should stop using these specific lots and contact the manufacturer for details.
cGMP deviations refer to failures in the manufacturing process that could affect product safety and quality. These deviations might mean the tablets do not meet the required standards for safety and effectiveness.
People who purchased Cystex Urinary Pan Relief tablets from Clarion Brands, LLC in the U.S. between the specified dates. Those with the listed lot numbers and expiration dates are most at risk.
Check the packaging for lot numbers: 19A043, 19A093, 19B062, 19C079, 19C080, 19D041, 19E035, 19E087, 19G084, 19H098, or 19H098A. The expiration dates range from January 2022 to September 2022.
Look for lot numbers listed in the recall notice: 19A043, 19A093, 19B062, 19C079, 19C080, 19D041, 19E035, 19E087, 19G084, 19H098, or 19H098A.
Reach out to Ultra Seal Corporation for further instructions on what to do with the recalled product.
Ultra Seal Corporation is recalling Cystex Urinary Pan Relief tablets due to cGMP deviations in manufacturing.
Affected lots include 19A043, 19A093, 19B062, 19C079, 19C080, 19D041, 19E035, 19E087, 19G084, 19H098, and 19H098A.
Check the packaging for the specific lot numbers listed in the recall notice and expiration dates from January 2022 to September 2022.
We’ve drafted a message you can send Ultra Seal to request your refund or repair — edit it as you like.
Subject: Recall D-0471-2022 — Ultra Seal Ultra Seal Hello, I own a Ultra Seal that is covered by recall D-0471-2022 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.
