HealthWise PERIOD PATCH Menstrual Pain Relief with Menthol 10% is recalled due to cGMP deviations. Affected units include NDC 71101-947-10, UPC 845717010726. Consumers should contact Unexo Life Sciences for details.
cGMP Deviations
HealthWise Menstrual Pain Relief patches with Menthol 10% are being recalled because of manufacturing quality issues. This recall affects products made for Veridian Healthcare in Gurnee, Illinois. The issue could lead to product failure, but the specific risk to consumers is not clearly described in the recall notice.
The recall mentions 'cGMP Deviations,' which refers to deviations in current Good Manufacturing Practices. These deviations could affect the product's safety and quality, but the specific hazard mechanism is not detailed in the recall notice.
Women who use HealthWise PERIOD PATCH Menstrual Pain Relief for menstrual pain relief are likely affected. Those who purchased the product from retailers in the U.S. are at risk of receiving the recalled items.
Check for the product name 'HealthWise PERIOD PATCH Menstrual Pain Relief, Menthol 10%, 10 patches per box.' The NDC code is 71101-947-10 and UPC is 845717010726.
Look for the NDC code 71101-947-10 and UPC 845717010726 on the packaging.
The recall is due to cGMP deviations, which are manufacturing quality issues. The specific risk to consumers is not clearly described in the notice.
Check for the NDC code 71101-947-10 and UPC 845717010726 on the packaging.
The recall notice does not specify a remedy, so contact Unexo Life Sciences directly for further instructions.
We’ve drafted a message you can send HealthWise to request your refund or repair — edit it as you like.
Subject: Recall D-0067-2025 — HealthWise HealthWise Hello, I own a HealthWise that is covered by recall D-0067-2025 from HealthWise. 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.