Independent register of U.S. FDA drug recalls · updated Oct 10, 2026
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Class I · High risk Terminated Initiated Jul 20, 2018 (8 years ago)

Dr. King's Advanced Arnica Super Arnica

Class I — High risk. Reasonable probability of serious harm or death.

Why it was recalled

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

Dr. King's Advanced Arnica Super Arnica, 59 mL, Manufactured by: King Bio, Inc. 3 Westside Dr. Asheville, NC 28806 Imported by Ambiental Solutions, Inc. Vancouver, BC, V5Y 1E6, DIN-HM 800774305 UPC 357955181224

Drug: Arnica

Recalling firm
King Bio Inc.
Origin
NC, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0960-2019 · FDA notice

Treat this as urgent. Class I means FDA judged there is a reasonable probability of serious harm. Find the lot number on your package; if it matches the recalled lots, do not take another dose before you have spoken to your pharmacist or prescriber - today, not next week. 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 all

Other recalls by King Bio Inc.

All 2018 recalls