The Recall Desk
ModerateFDA (Drugs)·D-0382-2025·Announced 2025-04-30

Rapidol Arnica Gel topical homeopathic medicine recalled for manufacturing violations

Pharmadel, LLC is recalling Rapidol Arnica Gel (2 oz, 57 g) distributed in Delaware due to manufacturing process deviations. The voluntary recall affects 6,048 bottles of lot EAG-01 with expiration date MAR 27.

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: This is an FDA Class II recall initiated voluntarily by the firm for manufacturing process deviations. The source text does not report any illnesses or injuries, and cGMP deviations without reported adverse health consequences are typically scored as Moderate under the rubric.

Plain-English summary

Pharmadel, LLC is voluntarily recalling Rapidol Arnica Gel, a topical homeopathic medicine, due to current good manufacturing practice (cGMP) deviations. The affected product is a 2 oz (57 g) topical gel with NDC 55758-403-02, lot EAG-01, expiration date MAR 27.

Approximately 6,048 bottles were distributed in Delaware. The recall was initiated on April 15, 2025, and classified as a Class II recall by the FDA on April 21, 2025.

Consumers who have purchased this product should stop using it and contact Pharmadel, LLC for instructions on return or disposal. The recall has been terminated as of January 8, 2026.

The recalled product

Product
Rapidol Arnica Gel, Topical Gel, Homeopathic Medicine, 2 oz (57 g), Distributed by: Pharmadel, New Castle, DE 19720, NDC 55758-403-02
Manufacturer
Pharmadel, LLC
Category
Drug — Topical / Homeopathic
Hazard
  • manufacturing-deviation
  • gmp-violation

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: EAG-01
  • EXP: MAR 27

Distribution

Distributed in 1 state:

  • DE

Related recalls

Same category