Planetary Herbals Ginseng Classic; Classic Chinese Energizer 710 mg; 60 and 120
Recalling firm: Threshold Enterprises Ltd
Why it was recalled
Product was inadvertently released prior to release of all QC testing. Testing had positive results for coliform growth.
Check your package
Compare the exact product and package details with the label you have.
ProductPlanetary Herbals Ginseng Classic; Classic Chinese Energizer 710 mg; 60 and 120 UPC 0 21078 10215 1 tablet bottles; 60 count - UPC 0 21078 10214 4; Product code PF0214 120 count - UPC 0 21078 10215; Product code PR0215.
UPC021078102144, 021078102151
FDA code information
60 count lot FG-86688, Exp. 5/21; 120 count lot FG-86689, Exp. 5/21.
Match the product, package size, and code together. A missing match does not guarantee safety.
Full FDA record and distribution details
Original product description
Planetary Herbals Ginseng Classic; Classic Chinese Energizer 710 mg; 60 and 120 UPC 0 21078 10215 1 tablet bottles; 60 count - UPC 0 21078 10214 4; Product code PF0214 120 count - UPC 0 21078 10215; Product code PR0215.
Extracted codes and context
| Type | Code / value | Context |
|---|---|---|
| UPC | 021078102144 | rgizer 710 mg; 60 and 120 UPC 0 21078 10215 1 tablet bottles; 60 count - UPC 0 21078 10214 4; Product code PF0214 120 count - UPC 0 21078 10215; Product code PR0215. |
| UPC | 021078102151 | ary Herbals Ginseng Classic; Classic Chinese Energizer 710 mg; 60 and 120 UPC 0 21078 10215 1 tablet bottles; 60 count - UPC 0 21078 10214 4; Product code PF0214 120 count - UPC 0 21078 10215; Product code PR0 |
Recall details
- Recall number
- F-3338-2017
- Event ID
- 77805
- FDA status
- Terminated
- Initiated
- Jun 16, 2017
- Reported
- Aug 9, 2017
- Classified
- Aug 2, 2017
- Terminated
- Aug 2, 2017
- Quantity
- 36 bottles - 7 x 120 count and 29 x 60 count.
- Location
- Scotts Valley, CA, United States
- Initiation type
- Voluntary: Firm initiated
- Notification
- Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Where it was distributed
CA, MN, WA, IL, PR, ME, SD.
FDA source record · F-3338-2017
Data updated September 16, 2026. View official FDA data ↗
Follow official FDA and manufacturer guidance.