Ultra Seal Corporation recalls FEM-PRIN Menstrual Relief tablets due to cGMP deviations. Affected lots manufactured for HARTHealth in Seattle, WA. No specific remedy stated in official recall.
cGMP deviations
Ultra Seal Corporation is recalling FEM-PRIN Menstrual Relief tablets that were manufactured for HARTHealth in Seattle, WA. The recall is due to cGMP deviations, which means the product may not meet quality standards. This could affect safety, but no specific remedy is provided in the official notice.
cGMP deviations refer to failures in the manufacturing quality control process. This could mean the product does not meet safety and quality standards, potentially leading to health risks. However, the specific risks are not detailed in the recall notice.
People who purchased the FEM-PRIN Menstrual Relief tablets from HARTHealth in Seattle, WA. Women using these products for menstrual relief are most at risk due to potential quality issues.
Check for the product name 'FEM-PRIN Menstrual Relief' tablets, 2-count packets. Look for the lot number AK9695 with an expiration date of 07/2022 manufactured for HARTHealth in Seattle, WA.
Identify the product name, lot number, and expiration date to confirm if it matches the recalled items.
The official recall does not state any remedy or action steps for affected products.
The recall mentions cGMP deviations, which indicate potential quality control issues in manufacturing, but specific health risks are not detailed.
Check for the product name 'FEM-PRIN Menstrual Relief' tablets, 2-count packets with lot number AK9695 and expiration date 07/2022 manufactured for HARTHealth in Seattle, WA.
We’ve drafted a message you can send Ultra Seal to request your refund or repair — edit it as you like.
Subject: Recall D-0509-2022 — Ultra Seal Ultra Seal Hello, I own a Ultra Seal that is covered by recall D-0509-2022 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.
