Severity
Moderate
ModerateClass IITerminated
FDA Food recall · Reported August 9, 2017
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.
Product was inadvertently released prior to release of all QC testing. Testing had positive results for coliform growth.
Threshold Enterprises Ltd recalled Planetary Herbals Ginseng Classic; Classic Chinese Energizer 710 mg; 60 and 120 UPC 0 2… - a moderate-severity action.
Planetary Herbals Ginseng Classic; Classic Chinese Energizer 710 mg; 60 and 120 UPC 0 2… was recalled by Threshold Enterprises Ltd in August 9, 2017. Reason: Product was inadvertently released prior to release of all QC testing. Testing had positive results for colif…. Check the official notice for the remedy. Verify recall #F-3338-2017 with the FDA Food before acting.
The recall
Threshold Enterprises Ltd issued this moderate-severity FDA Food recall-Product was inadvertently released prior to release of all QC testing. Testing had positive results for colif….
- Moderate
- severity level
- Class II
- classification
- August 9, 2017
- reported
Sourced from official FDA Food enforcement records. Verify recall #F-3338-2017 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
Recall Insight
This FDA Food action (record #F-3338-2017) was formally reported on August 9, 2017, with the manufacturer initiating the action on June 16, 2017. It is classified under Moderate severity (Class II), with a current status of Terminated. Threshold Enterprises Ltd is listed as the recalling firm, operating out of Scotts Valley, CA. Federal records list the affected scope as 36 bottles - 7 x 120 count and 29 x 60 count..
The documented reason for this recall is: Product was inadvertently released prior to release of all QC testing. Testing had positive results for coliform growth. Distribution data in the federal record shows the product reached: CA, MN, WA, IL, PR, ME, SD.. Distribution scope directly affects the consumer exposure window and determines whether a recall remains regional or escalates into a nationwide advisory.
Within the same product category the archive holds 6 closely related recalls - clustering in a narrow category often points to a systemic quality-control or supplier issue rather than a one-off defect. Always verify the recall number against the official agency record before acting.
Drugs & Medications recalls over time
Where this recall sits in its category - 14,436 drugs & medications recalls on record
Of 88,001 recalls with an agency hazard classification, 19,020 are high severity, 64,468 moderate, and 4,513 low. A further 16,157 CPSC/NHTSA recalls have no agency class and are excluded from this split. This recall is classified moderate severity.
Counts reflect market size and reporting activity, not inherent danger, we do not rank products by risk from raw recall volume.
Affected scope
36 bottles - 7 x 120 count and 29 x 60 count.
Related Recalls
6
0 from same agency
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.
Reason for recall
Product was inadvertently released prior to release of all QC testing. Testing had positive results for coliform growth.
Recall Profile
| Attribute | Value |
|---|---|
| Agency | U.S. Food and Drug Administration |
| Severity class | Moderate (Class II) |
| Status | Terminated |
| Recall number | F-3338-2017 |
| Date reported | August 9, 2017 |
| Date initiated | June 16, 2017 |
| Recalling firm | Threshold Enterprises Ltd |
| Firm location | Scotts Valley, CA |
| Affected scope | 36 bottles - 7 x 120 count and 29 x 60 count. |
| Distribution | CA, MN, WA, IL, PR, ME, SD. |
Profile values are sourced directly from the official FDA Food enforcement record. Source: U.S. Food and Drug Administration.
What to do with this recall
Match your product against the recall record, then act on the agency remedy.
- Check the recall number (F-3338-2017) and product description against the item you own. Search the archive
- Confirm the current status with FDA Food before acting, recall details can be updated.
- Follow the documented remedy (refund, replacement, repair, or disposal) rather than general advice. What to do next
This page summarizes the official FDA Food record for research and awareness; it is not legal, medical, or safety advice. Verify with the issuing agency before acting.
Frequently Asked Questions
What product was recalled? ▼
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.. Recalled by Threshold Enterprises Ltd. Units affected: 36 bottles - 7 x 120 count and 29 x 60 count..
Why was this product recalled? ▼
Product was inadvertently released prior to release of all QC testing. Testing had positive results for coliform growth.
Which agency issued this recall? ▼
This recall was issued by the FDA Food on August 9, 2017. Severity: Moderate. Recall number: F-3338-2017.
Where was the recalled product distributed? ▼
Distribution: CA, MN, WA, IL, PR, ME, SD..
How do I check if my product is affected by a recall? ▼
Check the product description and recall number (F-3338-2017) against your product. Visit the official FDA Food website for the most current information. You can also use our Recall Checker tool to search by product name or brand.
What are the health risks of consuming a recalled food product? ▼
Recalled food products may contain contaminants, undeclared allergens, or harmful bacteria such as Salmonella, Listeria, or E. coli. Consuming these products can cause foodborne illness ranging from mild gastrointestinal symptoms to serious conditions requiring hospitalization. If you have consumed a recalled food product and experience symptoms, contact your healthcare provider and report to the FDA via MedWatch.
Nationwide recalls with similar severity or category timing
Two federal-filing-derived peer sets for this notice, both outside the same recalling firm and filing state so the neighborhoods are not firm or geographic containment.
Similar severity · nearest report date
Same archive severity grade (Moderate), closest by report date among other firms and states.
Similar Drugs & Medications · nearest report date
Same product category, closest by report date among other firms and states (deduped against the severity set).
Nearby Recalls in This Category
Other recalls in the same product category, useful for spotting patterns across the same defect class or manufacturer.
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Every figure on PlainRecalls is rendered directly from official FDA, CPSC and NHTSA recall records, no number is typed in by an editor. This recall: FDA Food, reported August 9, 2017. Severity classes follow each agency's own taxonomy (FDA Class I/II/III; CPSC and NHTSA by hazard type), and related-recall context is computed across the full archive. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error. Data current as of August 2026.