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Stop using now Food recall · FDA · Published August 1, 2016

Life Rising DHZC-2 Dietary Supplement Recalled for Lead Contamination

Life Rising Corp recalls DHZC-2 dietary supplement due to lead contamination. Consumers should stop using the product immediately as lead exposure poses health risks.

🇺🇸 FDA recall #F-1725-2017FoodLife Rising ›
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Recalling firmLife Rising Corp S2131 S. Archer Avenue, Uite A · Chicago, IL 60616
✎ GovInfoNow plain-language explainer

What happened, in plain English

Life Rising Corp is recalling their DHZC-2 dietary supplement for lead contamination. This poses a health risk, especially for children and pregnant women who may be more vulnerable to lead exposure. Read more at govinfonow.com/recall/23680-life-rising-dhzc-2-dietary-supplement-recalled-for-lead-contamination.

Source Summary by GovInfoNow · govinfonow.com/recall/23680-life-rising-dhzc-2-dietary-supplement-recalled-for-lead-contamination · Updated October 9, 2026 · FDA enforcement record: FDA #F-1725-2017

Cite this page

“Life Rising DHZC-2 Dietary Supplement Recalled for Lead Contamination.” GovInfoNow, updated October 9, 2026. https://govinfonow.com/recall/23680-life-rising-dhzc-2-dietary-supplement-recalled-for-lead-contamination. Based on FDA recall #F-1725-2017 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-1725-2017%22&limit=1).

Why it’s dangerous

The supplement contains lead, a toxic heavy metal that can cause serious health issues including neurological damage, especially in children and pregnant women. Lead exposure can occur through ingestion of the supplement.

Who’s affected

Anyone who owns or uses the Life Rising DHZC-2 supplement. Children and pregnant women are at higher risk due to lead's potential to harm developing systems.

How to tell if you have this one

Look for the product in white plastic bottles with green lettering. The label states "LIFE RISING DHZC-2" and includes the description "blood circulation regulator (lower abdomen), Chinese Herbal Supplement, 60 tablets, life rising to higher well being". All lot codes are affected.

  • Brand
    Life Rising
  • Product
    The product is packaged in a white plastic bottle with green lettering. The label reads in part "LIFE RISING DHZC-2
  • Category
    Food
Based on the official FDA remedy

What to do — step by step

  1. Stop Using Now

    Immediately stop using the Life Rising DHZC-2 supplement as it contains lead, which can cause serious health issues.

Where it went and when

Where it was distributed

Distributed in 9 states, and outside the U.S.

Alaska: not listedAKMaine: not listedMEVermont: not listedVTNew Hampshire: not listedNHWashington: not listedWAIdaho: not listedIDMontana: not listedMTNorth Dakota: not listedNDMinnesota: not listedMNIllinois: yesILWisconsin: yesWIMichigan: yesMINew York: not listedNYRhode Island: not listedRIMassachusetts: not listedMAOregon: not listedORNevada: not listedNVWyoming: not listedWYSouth Dakota: not listedSDIowa: not listedIAIndiana: not listedINOhio: not listedOHPennsylvania: not listedPANew Jersey: not listedNJConnecticut: not listedCTCalifornia: yesCAUtah: not listedUTColorado: yesCONebraska: not listedNEMissouri: not listedMOKentucky: not listedKYWest Virginia: not listedWVVirginia: not listedVAMaryland: yesMDDelaware: not listedDEArizona: not listedAZNew Mexico: not listedNMKansas: not listedKSArkansas: yesARTennessee: not listedTNNorth Carolina: not listedNCSouth Carolina: not listedSCDistrict of Columbia: not listedDCOklahoma: yesOKLouisiana: not listedLAMississippi: not listedMSAlabama: not listedALGeorgia: not listedGAHawaii: not listedHITexas: not listedTXFlorida: yesFL

FDA distribution: “This product was shipped to IL, OK, FL, WI, MI, CA, MD, AR and CO. The firm did not ship any product to foreign consignees.” States read from FDA’s own wording; “not listed” means the notice does not name it.

States: Arkansas, California, Colorado, Florida, Illinois, Maryland, Michigan, Oklahoma, Wisconsin.

Recall timeline

FDA terminated this recall 2.6 years after the firm started it.

1. Firm started the recall: Aug 1, 201612. FDA classified it Class I: Mar 24, 201723. Published in FDA’s Enforcement Report: Apr 5, 201734. FDA terminated the recall: Mar 1, 2019420162019
  1. Firm started the recall
  2. FDA classified it Class I
  3. Published in FDA’s Enforcement Report
  4. FDA terminated the recall

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-1725-2017 (August 1, 2016) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-1725-2017 to see it in context.
  • Plain-language summary written by qwen3:4b on October 9, 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