Pharmadel recalls 100-count Rapidol Arnica Tablets due to cGMP deviations. Consumers should check product details and contact the company for guidance.
cGMP deviations
Pharmadel is recalling 100-count Rapidol Arn:ica Tablets because of manufacturing quality issues. This recall does not involve immediate safety risks but addresses potential product quality concerns.
The product was manufactured under cGMP (current Good Manufacturing Practice) deviations, which may affect quality but does not pose immediate safety risks. This issue relates to product quality rather than direct harm.
Homeopathic medicine users who purchased Rapidol Arnica Tablets from Pharmadel. Those most at risk are individuals using the product for medical purposes.
Check for the 100-count bottle labeled 'Rapidol Arnica Tablets, Homeopathic Medicine' with NDC 55758-405-99. The lot number is EAT-01 and expiration date is March 27.
Look for the NDC number 55758-405-99 on the bottle label to confirm it's the recalled product.
The recall is due to manufacturing quality issues, not immediate safety risks. The product is not considered dangerous under normal use.
Check for the NDC number 55758-405-99 on the bottle label. The lot number is EAT-01 and expiration date is March 27.
The recall does not specify a remedy, so contact Pharmadel directly for guidance.
We’ve drafted a message you can send Pharmadel to request your refund or repair — edit it as you like.
Subject: Recall D-0383-2025 — Pharmadel Pharmadel Hello, I own a Pharmadel that is covered by recall D-0383-2025 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.