Recall Register

Food recall: Life Rising TT Side Head Regulator, Chinese Herbal Supplement, 60 Tablets; Manufactured for: Ton Shen Health (USA)…

Class I FDA enforcement event 75560. Recall start date: . Status in the FDA record: Terminated. Termination date: .

Reason for recall, in the words of FDA

High levels of lead discovered in product.

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 28 Oct 2016. The firm address in the FDA record is in Chicago, IL. FDA put the recall in Class I. FDA event 75560 has 1 product record. The first FDA enforcement report date is 29 Mar 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.

Nationwide, Puerto Rico, Canada

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.

FDA event 75560: product records
Recall numberProductQuantityClassStatusReport date
F-1623-2017Life Rising TT Side Head Regulator, Chinese Herbal Supplement, 60 Tablets; Manufactured for: Ton Shen Health (USA), Chicago, IL, 60616; Made in China6,964 bottlesClass ITerminated29 Mar 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

Official channels

Cite this page

Recall Register. FDA enforcement event 75560. https://recallregister.com/fda/i/75560/. 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: Nationwide, Puerto Rico, Canada
What quantity of product is in FDA event 75560?
The FDA record gives this quantity: 6,964 bottles
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.