Life Rising Corp S Recall: The dietary supplement contains lead. - F-1725-2017
🇺🇸 United States
TerminatedClass I
Company
Life Rising Corp S
Product
The product is packaged in a white plastic bottle with green…
Recall date
August 1, 2016
Terminated
March 1, 2019
Source
FDA
Reason for recall
The dietary supplement contains lead.
- Recall initiated
- Reported by source
- Recall terminated
Recalled products
Product description
UPC
Quantity
Lot / code information
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
616042102727
216 bottles, 60 tablets per bottle
All lot codes
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.
Official source record
Agency
FDA
Dataset
FDA Food Enforcement (Recalls)
Recall number
F-1725-2017
Event ID
74929
Status
Terminated
Classification
Class I
Company
Life Rising Corp S
Product description
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
Quantity
216 bottles, 60 tablets per bottle
Reason
The dietary supplement contains lead.
Recall initiation date
August 1, 2016
Report date
April 5, 2017
Classification date
Not published in this source record
Termination date
March 1, 2019
Distribution pattern
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.
UPC, lot, and code information
UPC 616042102727; All lot codes
Voluntary or mandated
Voluntary: Firm initiated
Initial notification method
Telephone
Source last updated
Not tracked separately from the Public Health Trace retrieval date below
A map highlighting the states named in the source's distribution description.
Distributed
No data published
Shading reflects state-level totals only, as published by the source. It does not imply
county-level or point-level precision.
Distribution map
State
Distributed
Illinois
1
Oklahoma
1
Florida
1
Wisconsin
1
Michigan
1
California
1
Maryland
1
Arkansas
1
Colorado
1
States shown are extracted from the source's free-text distribution description above; a narrative
description (e.g. "distributed nationwide") may not list individual states to extract.
View raw source data
-- the machine-readable record this page's information was built from.
Retrieved by Public Health Trace:
Frequently asked questions
What does a Class I mean?
FDA classifies this recall as Class I. See how to read an FDA recall record (linked above) for what each classification level means.
Is this recall still active?
According to FDA, this recall's status is "Terminated." Always confirm the current status using the source links below, since status can change after Public Health Trace last retrieved this record.
What should I do if I have this product?
Follow the responsible agency's published instructions, linked below -- recall guidance is set by that agency, not by Public Health Trace.
Official guidance and record verification
Public Health Trace does not provide medical advice -- review the linked official source below for
current, authoritative information.
How to interpret this historical record
This record is preserved as published by FDA, as of March 1, 2019.
Status as reported: Terminated.
This page does not imply a current danger or a current consumer instruction -- review the official source for the most current information.
This summary is based on the official source record referenced above. Public Health Trace does not state that any company
or product is unsafe beyond what the official source has published.
Read the full medical disclaimer.