Arnica Power
Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.
Why it was recalled
CGMP Deviations: products manufactured by contract manufacturer under conditions that could result in possible microbial contamination.
Cause type: Microbial contamination
Bacteria, mold, yeast or other microorganisms detected in the product. Contamination can occur from water systems, equipment or handling, and can cause infection. All microbial contamination recalls.
What was recalled
Arnica Power, Homeopathic Oral Spray, 1.38 fl. oz (41ml), Manufactured for Sprayology Gaithersburg. MD 20879.NDC 61096-0032-1
Compare with the code on your package — it is the most precise check available.
Drug: Arnica
- Recalling firm
- Sprayology
- NDC code
- 61096-0032-1
- Origin
- MD, United States
- Initiated by
- Voluntary: Firm initiated
- FDA recall number
- D-0117-2019 · FDA notice
Check, then ask. Class II means harm is possible but usually temporary or reversible. Find the lot number on your package; if it matches, ask your pharmacist about a replacement. Do not simply stop a prescribed medication on your own - the gap can be riskier than the recall. This recall is now terminated, which means the firm has finished removing the affected product; anything on pharmacy shelves today should be unaffected.
Other Arnica recalls
See allRapidol Arnica Tablets
cGMP deviations
Rapidol Arnica Gel
cGMP deviations
Arnica 7 Cream
cGMP deviations
Kanjo Homeopathic Pain Relief Cream With Arnica
cGMP deviations
Other recalls by Sprayology
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CGMP Deviations: products manufactured by contract manufacturer under conditions that could result in possible microbial contamination.
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CGMP Deviations: products manufactured by contract manufacturer under conditions that could result in possible microbial contamination.
Acne Tonic Homeopathic Oral Spray 1.38 fl. oz.
CGMP Deviations: products manufactured by contract manufacturer under conditions that could result in possible microbial contamination.
Body Skin Tonic
CGMP Deviations: products manufactured by contract manufacturer under conditions that could result in possible microbial contamination.
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