Life Rising TT Side Head Regulator Contains Lead - Recall
Life Rising Corp recalls Chinese herbal supplement with lead contamination. High lead levels found in 60-tablet product. Consumers should stop using immediately.
Stop using this now
High levels of lead discovered in product.
Contact the company
What happened, in plain English
Life Rising Corp recalled their TT Side Head Regulator herbal supplement due to high lead levels. This poses a health risk, especially for children and pregnant women who may be more vulnerable to lead poisoning. Read more at govinfonow.com/recall/22959-life-rising-tt-side-head-regulator-contains-lead-recall.
Source Summary by GovInfoNow · govinfonow.com/recall/22959-life-rising-tt-side-head-regulator-contains-lead-recall · Updated October 9, 2026 · FDA enforcement record: FDA #F-1623-2017
Cite this page
“Life Rising TT Side Head Regulator Contains Lead - Recall.” GovInfoNow, updated October 9, 2026. https://govinfonow.com/recall/22959-life-rising-tt-side-head-regulator-contains-lead-recall. Based on FDA recall #F-1623-2017 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-1623-2017%22&limit=1).
Why it’s dangerous
Lead is a toxic heavy metal that can cause serious health problems, including neurological damage and developmental delays in children. High lead levels in this herbal supplement pose a risk of lead poisoning, especially with regular consumption.
Who’s affected
Anyone who owns the Life Rising TT Side Head Regulator herbal supplement. Children and pregnant women are at higher risk due to lead's potential to cause developmental issues.
How to tell if you have this one
Look for the product name 'Life Rising TT Side Head Regulator' with 60 tablets. The product was manufactured for Ton Shen Health in Chicago, IL, and sold in the US. All lots are affected.
- Brand
Life Rising- Category
Food
What to do — step by step
Stop Using It Now
Immediately stop using the Life Rising TT Side Head Regulator herbal supplement as it contains high levels of lead.
Where it went and when
Where it was distributed
Distributed nationwide, and outside the U.S.
FDA distribution: “Nationwide, Puerto Rico, Canada” States read from FDA’s own wording; “not listed” means the notice does not name it.
Distributed nationwide, and outside the U.S.
Recall timeline
FDA terminated this recall 2.3 years after the firm started it.
- Firm started the recall
- FDA classified it Class I
- Published in FDA’s Enforcement Report
- FDA terminated the recall
Dates from the agency record only; steps without a date are left out.
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Where this comes from
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
- Official source: FDA Recall #F-1623-2017 (October 28, 2016) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-1623-2017 to see it in context.
- Plain-language summary written by qwen3:4b on October 9, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
- GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.