CLASS I Food recall · Reported 5 Apr 2017 · FDA Enforcement Report

The product is recalled by Life Rising Corp S

Life Rising Corp S is recalling The product is, distributed in 9 states. The recall was initiated on 1 Aug 2016 and the FDA has classified it as Class I.

Check your package

Lot, batch or date codesAll lot codes
Quantity recalled216 bottles, 60 tablets per bottle

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

Recall details

Recall number
F-1725-2017
FDA event ID
74929
Recalling firm
Life Rising Corp S, Chicago, IL
Classification
Class I
Status
Terminated
Recall initiated
1 Aug 2016
FDA classified
24 Mar 2017
Reported
5 Apr 2017
Type
Voluntary: Firm initiated
Customers notified by
Telephone
Reason category
Foreign Material
Product category
Herbal Supplements

Timeline

1 Aug 2016Recall initiated by company
24 Mar 2017Classified by FDA+235 days
5 Apr 2017Published in enforcement report+12 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

The dietary supplement contains lead.

Foreign material recalls cover pieces of metal, plastic, glass, wood or other objects that got into the product during processing and could cause injury if eaten.

Product as listed by the FDA

The product is packaged in a white plastic bottle with green lettering. The label reads in part "LIFE RISING DHZC-2, blood circulation regulator (lower abdomen), Chinese Herbal Supplement, 60 tablets, life rising to higher well being", UPC: 616042102727

Where it was distributed

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.

ArkansasCaliforniaColoradoFloridaIllinoisMarylandMichiganOklahomaWisconsin

Questions about this recall

Is The product is recalled?

Yes. Life Rising Corp S recalled The product is on 1 Aug 2016. The recall is Class I and its status is Terminated. Recall number F-1725-2017.

Why was it recalled?

The dietary supplement contains lead.

Which lots are affected?

All lot codes

Where was it sold?

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.

What should I do if I have it?

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

What does Class I mean?

Class I is the most serious FDA recall category: there is a reasonable probability that using the product will cause serious health consequences or death.

Read the official FDA notice · Source record retrieved 21 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

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