Wisconsin Pharmacal Yeast Arrest Suppositories Recall: CPG Violations
Wisconsin Pharmacal recalls Yeast Arrest vaginal suppositories due to cGMP violations. Products sold in 14-count and 28-count cartons with specific lot numbers. No remedy provided in official notice.
Recall notice
cGMP violations
Contact the company
What happened, in plain English
Wisconsin Pharmacal is recalling Yeast Arrest vaginal suppositories because of cGMP violations. This means the product may not meet quality standards and could pose safety risks. Consumers should check their product details to see if they are affected. Read more at govinfonow.com/recall/37698-wisconsin-pharmacal-yeast-arrest-suppositories-recall-cpg-violations.
Source Summary by GovInfoNow · govinfonow.com/recall/37698-wisconsin-pharmacal-yeast-arrest-suppositories-recall-cpg-violations · Updated October 5, 2026 · FDA enforcement record: FDA #D-0781-2020
Cite this page
“Wisconsin Pharmacal Yeast Arrest Suppositories Recall: CPG Violations.” GovInfoNow, updated October 5, 2026. https://govinfonow.com/recall/37698-wisconsin-pharmacal-yeast-arrest-suppositories-recall-cpg-violations. Based on FDA recall #D-0781-2020 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0781-2020%22&limit=1).
Why it’s dangerous
The recall is due to cGMP (current Good Manufacturing Practice) violations, which indicate the product may not meet quality and safety standards. These violations could lead to potential risks such as improper potency or contamination, though the exact hazard is not specified in the notice.
Who’s affected
Women who purchased Yeast Arrest vaginal suppositories from 2020 to 2021 are likely affected. Those using the product for vaginal support may be at higher risk due to potential quality issues.
How to tell if you have this one
Check for 14-count or 28-count cartons with lot numbers 81827 (exp 8/2020), 111872 (exp 11/2020), 41970 (exp 4/2021), or 519104 (exp 5/2021). Products were sold by Wisconsin Pharmacal in the United States between 2020 and 2021.
- Brand
Wisconsin Pharmacal- Category
Drug
What to do — step by step
Check Product Details
Identify if your suppositories match the recalled lot numbers and packaging described in the notice.
Where it went and when
Where it was distributed
Distributed in Oregon.
FDA distribution: “OR” States read from FDA’s own wording; “not listed” means the notice does not name it.
States: Oregon.
Recall timeline
FDA terminated this recall 12 months after the firm started it.
- Firm started the recall
- FDA classified it Class II
- Published in FDA’s Enforcement Report
- FDA terminated the recall
Dates from the agency record only; steps without a date are left out.
Similar recalls
Latest drug recalls
Keep exploring
Where this comes from
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.
- Official source: FDA Recall #D-0781-2020 (November 14, 2019) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-0781-2020 to see it in context.
- Plain-language summary written by qwen3:4b on October 5, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
- GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.