Life Rising Corp S Recall: High levels of lead discovered in product. - F-1623-2017

United States

TerminatedClass I

Company: Life Rising Corp S
Product: Life Rising TT Side Head Regulator, Chinese Herbal Supplemen…
Recall date: October 28, 2016
Terminated: March 1, 2019
Source: FDA

Reason for recall

High levels of lead discovered in product.

October 28, 2016 - Recall initiated
March 29, 2017 - Reported by source
March 1, 2019 - Recall terminated

Recalled products
Product description	UPC	Quantity	Lot / code information
Life Rising TT Side Head Regulator, Chinese Herbal Supplement, 60 Tablets; Manufactured for: Ton Shen Health (USA), Chicago, IL, 60616; Made in China	Not published in this source record	6,964 bottles	All lots

Distribution

Nationwide
Puerto Rico
Canada

Official source record

Agency: FDA
Dataset: FDA Food Enforcement (Recalls)
Recall number: F-1623-2017
Event ID: 75560
Status: Terminated
Classification: Class I
Company: Life Rising Corp S
Product description: Life Rising TT Side Head Regulator, Chinese Herbal Supplement, 60 Tablets; Manufactured for: Ton Shen Health (USA), Chicago, IL, 60616; Made in China
Quantity: 6,964 bottles
Reason: High levels of lead discovered in product.
Recall initiation date: October 28, 2016
Report date: March 29, 2017
Classification date: Not published in this source record
Termination date: March 1, 2019
Distribution pattern: Nationwide, Puerto Rico, Canada
UPC, lot, and code information: All lots
Voluntary or mandated: Voluntary: Firm initiated
Initial notification method: Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Source last updated: Not tracked separately from the Public Health Trace retrieval date below
Public Health Trace retrieval date: July 18, 2026 ET

Responsible company: Life Rising Corp S

Other recalls from Life Rising Corp S

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FDA Recall United States TerminatedTerminated: March 1, 2019Historical recordClass I

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Product: Product is packaged in a white plastic bottle with green let…
Published: March 29, 2017
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Where this information comes from

View FDA enforcement record -- the specific openFDA record this summary was built from.

This record comes from FDA's Enforcement Report database. Not every Enforcement Report record has a separate FDA.gov recall-announcement page.

FDA Enforcement Reports -- FDA's general, official recall and enforcement information. See FDA Enforcement Reports versus recall announcements for how that database differs from a press-release-style announcement.

New to reading a recall record? See how to read an FDA recall record and what recall statuses mean.

Technical source data

View raw source data -- the machine-readable record this page's information was built from.

Retrieved by Public Health Trace: July 18, 2026 ET

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

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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.

View the official FDA source

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