Food recall: The product is packaged in a white plastic bottle with green lettering. The label reads in part "LIFE RISING DHZC-2…
Class I FDA enforcement event 74929. Recall start date: . Status in the FDA record: Terminated. Termination date: .
Reason for recall, in the words of FDA
The dietary supplement contains lead.
Class I, in the words of FDA
a situation in which there is a reasonable probability that the use of or exposure to a violative product will cause serious adverse health consequences or death
Life Rising Corp S started this food recall on 1 Aug 2016. The firm address in the FDA record is in Chicago, IL. FDA put the recall in Class I. FDA event 74929 has 1 product record. The first FDA enforcement report date is 5 Apr 2017. The record gives the status Terminated, with the termination date 1 Mar 2019.
It is important to note that most of the time recall classifications are determined after the recalling firm provides all of the information needed to determine the risk posed to public health. The classification and posting in the FDA Enforcement Report should not be seen as an expansion or change to a firm’s voluntary public warning.
FDA publishes these words. Source: FDA, Enforcement Reports, Important Note, read on . openFDA export of .
Distribution
In the words of FDA.
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.
Recalling firm
Life Rising Corp S, Chicago, IL.
Recalling firm: The firm that the FDA record names for a recall.
FDA records how the recall started: Voluntary: Firm initiated.
Products
1 product record in the event.
| Recall number | Product | Quantity | Class | Status | Report date |
|---|---|---|---|---|---|
| F-1725-2017 | 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 | 216 bottles, 60 tablets per bottle | Class I | Terminated | 5 Apr 2017 |
openFDA, about the status: FDA does not update the status of a recall after the recall has been classified according to its level of hazard. As such, the status of a recall (open, completed, or terminated) will remain unchanged after published in the Enforcement Reports.
Source: openFDA, Drug Recall Enforcement Reports, Disclaimer.
Enforcement report: The FDA publication that lists recalls. It has one record for each product of a recall.
Enforcement event: All the product records that have one FDA event number. This site shows one event on one page.
Class I: The highest of the three FDA recall classes.
The event in context
- Food events that started in 2016
- 799
- Share of these events in Class I
- 52%
- Product records in this event
- 1Median of the firm: 1
- Events of the firm on the register
- 3
Other events of the firm
| Initiated | Product (first record) | Type | Class | Records |
|---|---|---|---|---|
| 28 Oct 2016 | Life Rising TT Side Head Regulator, Chinese Herbal Supplement, 60 Tablets; Manufactured for: Ton Shen Health (USA), Chic | Food | Class I | 1 |
| 14 Sep 2016 | Product is packaged in a white plastic bottle with green lettering. The label reads in part LIFE RISING, Chinese Herbal | Food | Class I | 1 |
Official channels
- FDA enforcement report F-1725-2017The FDA record of the first product of this event.
- FDA: recalls, market withdrawals and safety alertsThe recall notices on the FDA site.
- FDA: report a problemThe FDA page that shows where a report about a product goes.
Follow by RSS:Food, drug and device recallsFDA Class I recalls
Cite this page
Recall Register. FDA enforcement event 74929. https://recallregister.com/fda/i/74929/. Source: openFDA enforcement reports. Data through .
Sources
- Source
- openFDA food enforcement reports
- Licence
- CC0 1.0
- Export date
- 28 Sep 2026
- Newest FDA report date on the register
- 23 Sep 2026
FDA has one record for each product. This site puts the records with the same event number on one page. The class of the event is the highest class of its records. How the register is made. Report an error.
Questions
- Where was the product distributed?
- The FDA record gives this 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.
- What quantity of product is in FDA event 74929?
- The FDA record gives this quantity:
216 bottles, 60 tablets per bottle
- How did the recall start?
- The FDA record says:
Voluntary: Firm initiated
- How many food recalls of 2016 have the same class?
- 52% of the 799 food events that started in 2016 are in Class I.