The Recall Desk
ModerateFDA (Drugs)·D-0383-2025·Announced 2025-04-30

Rapidol Arnica Tablets recalled due to manufacturing deviations

Pharmadel is recalling 6,048 bottles of Rapidol Arnica Tablets homeopathic medicine due to current good manufacturing practice (cGMP) deviations. The recall affects bottles with lot EAT-01, expiration date March 27, distributed in Delaware.

What this means for you

Minor labeling or packaging issue, or a voluntary precautionary recall. Risk of harm is low but real — follow the manufacturer's instructions.

Our severity reasoning: The FDA classified this as Class II. The source text identifies cGMP deviations as the reason but does not report any actual illnesses, injuries, or hospitalization; the hazard is process-related and precautionary in nature, supporting a Moderate severity rating.

Plain-English summary

Pharmadel, LLC is recalling Rapidol Arnica Tablets, a homeopathic medicine sold in 100-count bottles with NDC 55758-405-99. The recall involves 6,048 bottles with lot number EAT-01 and expiration date March 27, distributed in Delaware.

The recall was initiated due to current good manufacturing practice (cGMP) deviations identified during manufacturing operations. This is a voluntary recall initiated by the firm and classified by the FDA as Class II.

Consumers who have purchased this product should stop using it. The recall was terminated as of January 8, 2026.

The recalled product

Product
Rapidol Arnica Tablets, Homeopathic Medicine, 100-count bottle, Distributed by: Pharmadel, New Castle, DE 19720, NDC 55758-405-99
Manufacturer
Pharmadel, LLC
Category
Drug — Homeopathic Medicine
Hazard
  • cgmp-deviation

Is your product affected?

Check your packaging against the codes below. If any of them match, the product is part of this recall.

Lot numbers (3)

  • Lot
  • expiry: EAT-01
  • EXP: MAR 27

Distribution

Distributed in 1 state:

  • DE

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