Life Rising Chest Relief Capsules May Contain Lead - Recall
Ton Shen Health recalls Life Rising Chest Relief capsules due to potential lead contamination. All lots are affected. Consumers should contact the company for details.
Lower-risk recall
Product potentially contaminated with lead.
Contact the company
What happened, in plain English
Ton Shen Health is recalling Life Rising Chest Relief capsules because they may contain lead. This contamination poses a health risk, especially for children and pregnant women who are more vulnerable to lead poisoning. Read more at govinfonow.com/recall/21908-life-rising-chest-relief-capsules-may-contain-lead-recall.
Source Summary by GovInfoNow · govinfonow.com/recall/21908-life-rising-chest-relief-capsules-may-contain-lead-recall · Updated October 8, 2026 · FDA enforcement record: FDA #F-2167-2017
Cite this page
“Life Rising Chest Relief Capsules May Contain Lead - Recall.” GovInfoNow, updated October 8, 2026. https://govinfonow.com/recall/21908-life-rising-chest-relief-capsules-may-contain-lead-recall. Based on FDA recall #F-2167-2017 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-2167-2017%22&limit=1).
Why it’s dangerous
Lead is a toxic heavy metal that can cause serious health issues, especially in children and pregnant women. Even small amounts of lead in food products can lead to lead poisoning, which affects the nervous system and development.
Who’s affected
People who bought Life Rising Chest Relief capsules from any retailer. Children and pregnant women are at higher risk due to lead's impact on developing bodies.
How to tell if you have this one
Check for Life Rising Chest Relief capsules with 54 capsules per bottle. All lots are affected, so no specific lot numbers are needed.
- Brand
Ton Shen Health- Category
Food
What to do — step by step
Contact Manufacturer
Reach out to Ton Shen Health directly for guidance on next steps.
Where it went and when
Where it was distributed
Distributed in Illinois.
FDA distribution: “IL” States read from FDA’s own wording; “not listed” means the notice does not name it.
States: Illinois.
Recall timeline
FDA terminated this recall 5.6 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-2167-2017 (March 30, 2017) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-2167-2017 to see it in context.
- Plain-language summary written by qwen3:4b on October 8, 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.