Eugene Oregon, Inc.
Eugene Oregon, Inc. appears in FDA public data with 3 recalls — including 3 Class I (most serious) —, 0 510(k) clearances, 1 FDA inspection, and 0 compliance actions on record. Its most recent recall (D-1614-2014, Class I) was initiated on May 5, 2014.
Summary
- Total Recalls
- 3 (3 Class I)
- 510(k) Clearances
- 0
- Inspections
- 1
- Compliance Actions
- 0
Recent Recalls
| Number | Class | Product | Date |
|---|---|---|---|
| D-1614-2014 | Class I | MOJO RISEN, 650 mg, 2 capsule per pouch, Distributed by: Mojo Risen, LLC, Springville, UT 84663 | May 5, 2014 |
| D-1613-2014 | Class I | Black Ant, 2800 mg, four capsules per box, Manufacturer Qinghai Baojiantang Pharmaceutical Co., Ltd. | May 5, 2014 |
| D1612-2014 | Class I | AFRICAN BLACK ANT, 2800 mg, 6 capsules per box, produced by: Qinghan Hongwei Bioengineering Company, | May 5, 2014 |