Dr — Class I drug recall D-0960-2019
Terminated recall by King Bio Inc., reported 2019-03-20, distributed nationwide. Microbial contamination
| Recall number | D-0960-2019 |
|---|---|
| Product type | Drug |
| Classification | Class I |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | King Bio Inc., Asheville, NC, United States |
| Recall initiated | 2018-07-20 |
| Classified | 2019-03-08 |
| Reported by FDA | 2019-03-20 |
| Terminated | 2022-01-19 |
| Distributed | Nationwide (US) |
| Countries outside the US | AU, CA |
| Quantity | 1,110 bottles |
| Reason classes | microbial contamination |
| UPC / GTIN / UDI-DI | 00357955181224 |
| Lot numbers | 01/20, 013117P |
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 for recall
Microbial contamination
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/D-0960-2019. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.