Pharmadel recalls homeopathic UTI relief tablets due to manufacturing quality issues. Affected products have NDC 55758-406-30 and lot UDE-01 expiring OCT 26.
cGMP deviations
Pharmadel is recalling homeopathic urinary tract infection relief tablets because of manufacturing quality deviations. This means the product may not be safe or effective as intended.
The product was made under conditions that don't meet current good manufacturing practices. This could mean the tablets might not work properly or could be unsafe for consumption.
People who purchased the Urodel UTI relief tablets with NDC 55758-406-30 and lot number UDE-01 expiring October 26, 2024, are affected. Those using the product for urinary tract symptoms may be at risk.
Check for the product name 'Urodel, Urinary Tract Infection Symptoms Relief', 30 chewable tablets per bottle, NDC 55758-406-30, and lot number UDE-01 expiring October 26, 2024.
Look for NDC 55758-406-30 and lot number UDE-01 expiring October 26, 2024 on the bottle.
The recall is due to manufacturing quality deviations, but the official notice doesn't specify if the product is safe or effective.
The recall record doesn't state a remedy, so no specific action is required beyond checking product details.
Check for NDC 55758-406-30 and lot number UDE-01 expiring October 26, 2024 on the bottle.
We’ve drafted a message you can send Pharmadel to request your refund or repair — edit it as you like.
Subject: Recall D-0384-2025 — Pharmadel Pharmadel Hello, I own a Pharmadel that is covered by recall D-0384-2025 from Pharmadel. 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.
