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Lower risk Food recall · FDA · Published June 16, 2017

Planetary Herbals Ginseng Products Recall: Coliform Contamination Risk

Planetary Herbals recalls two ginseng supplement products due to coliform bacteria contamination detected during testing. Consumers should check product codes and lot numbers for affected items.

🇺🇸 FDA recall #F-3338-2017FoodPlanetary Herbals ›
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Recalling firmThreshold Enterprises Ltd23 Janis Way · Scotts Valley, CA 95066-3506
✎ GovInfoNow plain-language explainer

What happened, in plain English

Planetary Herbals is recalling two ginseng supplement products because testing found coliform bacteria growth. This contamination could pose health risks if consumed, so affected consumers should stop using the products. Read more at govinfonow.com/recall/20738-planetary-herbals-ginseng-products-recall-coliform-contamination-risk.

Source Summary by GovInfoNow · govinfonow.com/recall/20738-planetary-herbals-ginseng-products-recall-coliform-contamination-risk · Updated October 8, 2026 · FDA enforcement record: FDA #F-3338-2017

Cite this page

“Planetary Herbals Ginseng Products Recall: Coliform Contamination Risk.” GovInfoNow, updated October 8, 2026. https://govinfonow.com/recall/20738-planetary-herbals-ginseng-products-recall-coliform-contamination-risk. Based on FDA recall #F-3338-2017 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-3338-2017%22&limit=1).

Why it’s dangerous

The products were contaminated with coliform bacteria during manufacturing before full quality testing was completed. Coliform bacteria can cause gastrointestinal issues if ingested, but the risk is low since the products were only tested for a short time.

Who’s affected

Consumers who purchased Planetary Herbals Ginseng Classic or Classic Chinese Energizer 710 mg supplements with the specified UPC codes and lot numbers are affected. People taking these supplements regularly are most at risk.

How to tell if you have this one

Check for product codes: UPC 02107810215 (60-count) or UPC 02107810214 (120-count). Lot numbers FG-86688 (60-count) or FG-86689 (120-count) with expiration dates of May 2021.

  • Brand
    Planetary Herbals
  • Product
    Planetary Herbals Ginseng Classic; Classic Chinese Energizer 710 mg; 60 and 120 UPC 0 21078 10215 1 tablet bottles; 60
  • Category
    Food
Based on the official FDA remedy

What to do — step by step

  1. Check Product Details

    Verify your product's UPC code and lot number to confirm if it's affected.

Where it went and when

Where it was distributed

Distributed in 6 states and Puerto Rico.

Alaska: not listedAKMaine: yesMEVermont: not listedVTNew Hampshire: not listedNHWashington: yesWAIdaho: not listedIDMontana: not listedMTNorth Dakota: not listedNDMinnesota: yesMNIllinois: yesILWisconsin: not listedWIMichigan: not listedMINew York: not listedNYRhode Island: not listedRIMassachusetts: not listedMAOregon: not listedORNevada: not listedNVWyoming: not listedWYSouth Dakota: yesSDIowa: not listedIAIndiana: not listedINOhio: not listedOHPennsylvania: not listedPANew Jersey: not listedNJConnecticut: not listedCTCalifornia: yesCAUtah: not listedUTColorado: not listedCONebraska: not listedNEMissouri: not listedMOKentucky: not listedKYWest Virginia: not listedWVVirginia: not listedVAMaryland: not listedMDDelaware: not listedDEArizona: not listedAZNew Mexico: not listedNMKansas: not listedKSArkansas: not listedARTennessee: not listedTNNorth Carolina: not listedNCSouth Carolina: not listedSCDistrict of Columbia: not listedDCOklahoma: not listedOKLouisiana: not listedLAMississippi: not listedMSAlabama: not listedALGeorgia: not listedGAHawaii: not listedHITexas: not listedTXFlorida: not listedFLPuerto Rico: yesPR

FDA distribution: “CA, MN, WA, IL, PR, ME, SD.” States read from FDA’s own wording; “not listed” means the notice does not name it.

States: California, Illinois, Maine, Minnesota, Puerto Rico, South Dakota, Washington.

Recall timeline

FDA terminated this recall 47 days after the firm started it.

1. Firm started the recall: Jun 16, 201712. FDA classified it Class II: Aug 2, 201723. FDA terminated the recall: Aug 2, 201734. Published in FDA’s Enforcement Report: Aug 9, 201742017
  1. Firm started the recall
  2. FDA classified it Class II
  3. FDA terminated the recall
  4. Published in FDA’s Enforcement Report

Dates from the agency record only; steps without a date are left out.

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Where this comes from

The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.

  • Official source: FDA Recall #F-3338-2017 (June 16, 2017) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-3338-2017 to see it in context.
  • Plain-language summary written by qwen3:4b on October 8, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
  • GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.
GovInfoNow is an independent guide. We are not FDA or any government agency. Always confirm details with the official recall.Data: CPSC · FDA · NHTSA · USDA