FDA Drug recall D-0960-2019
Dr. King's Advanced Arnica Super Arnica, 59 mL, Manufactured by: King Bio, Inc. 3 Westside Dr. Asheville, NC 28806 Imported by Ambiental So…
- FDA Drug
- Class I
- terminated
- Published 2019-03-20
On 2019-03-20 the FDA classified a Class I recall of Dr. King's Advanced Arnica Super Arnica, 59 mL, Manufactured by: King Bio, Inc. 3 Westside Dr. Asheville, NC 28806 Imported by Ambiental So… by King Bio, citing microbial contamination.
Read the official FDA Drug notice
| Agency | FDA Drug |
|---|---|
| Recall number | D-0960-2019 |
| Classification | Class I |
| Status | terminated |
| Initiated | 2018-07-20 |
| Published | 2019-03-20 |
| Last updated | 2026-09-13 11:52 UTC |
| Company | King Bio |
| Distribution | US |
Product
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
Reason
Microbial contamination
Identifiers
| upc | 357955181224 |
|---|---|
| code_info | Lot: 013117P Exp. 01/20 |
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:52 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0960-2019%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.