Skip to content
Stop using now Food recall · FDA · Published May 2, 2019

Life Rising Holder-W Warmer Capsules Recall: High Lead Levels

Life Rising Corporation recalls 54-count Holder-W Warmer capsules purchased before May 2, 2019 due to high lead levels. Consumers should stop using these products immediately.

🇺🇸 FDA recall #F-1394-2019FoodLife Rising ›
Take action

Contact the company

Recalling firmLife Rising Corporation7884 S Quincy St · Willowbrook, IL 60527-8429
✎ GovInfoNow plain-language explainer

Life Rising Corporation is recalling 54-count Holder-W Warmer capsules bought before May 2, 2019 because they contain high lead levels. This poses a health risk, especially for children who might ingest the product. Read more at govinfonow.com/recall/17530-life-rising-holder-w-warmer-capsules-recall-high-lead-levels.

Source Summary by GovInfoNow · govinfonow.com/recall/17530-life-rising-holder-w-warmer-capsules-recall-high-lead-levels · Updated October 5, 2026 · FDA enforcement record: FDA #F-1394-2019

Cite this page

“Life Rising Holder-W Warmer Capsules Recall: High Lead Levels.” GovInfoNow, updated October 5, 2026. https://govinfonow.com/recall/17530-life-rising-holder-w-warmer-capsules-recall-high-lead-levels. Based on FDA recall #F-1394-2019 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-1394-2019%22&limit=1).

The Food and Drug Administration announced on May 2, 2019, that Life Rising Corporation voluntarily recalled Life Rising Holder-W Holder Warmer capsules due to high lead levels. The recall affects 54-count bottles sold before May 2, 2019.

How to tell if you have it

  • Brand: Life Rising
  • Product: Life Rising Holder-W Holder Warmer capsules, 54 count bottle
  • Quantity: 9 bottles
  • Sold: Mostly locally in the Chicago area at HoliCare clinics and via mail orders
  • Purchase date: Before May 2, 2019

The hazard

The recalled products contain high lead levels. The FDA classified this as a Class I recall.

Context

GovInfoNow's records show other recent recalls of similar products include Venzu Traders Cinnamon Powder Recall (2025-11-14), U.S. Trading Company Dragonfly Thai Ginger Powder Recall (2026-05-15), and Gusto Group Shrimp Paste Recall (2025-11-19).

How to tell if you have this one

Check for the 54-count Holder-W Warmer capsules with the Life Rising brand. Products purchased before May 2, 2019 are affected.

  • Brand
    Life Rising
  • Category
    Food
FDA recall event · 3 products

All 3 products in this recall

FDA lists each product line separately under one recall event. Check your product description, lot or code numbers against each row. Every row shares the hazard and remedy on this page.

  • Status
    Terminated
  • Distribution
    The recalled products were mostly sold locally in the Chicago area at HoliCare clinics and a limited quantity were also distributed through mail orders.
Recall numberProduct, codes & lotsQuantityClass
F-1394-2019Life Rising Holder-W Holder Warmer capsules, 54 count bottle; all products purchased before May 2, 20199 bottlesClass I
F-1395-2019Life Rising NECK-ND Neck Clear capsules, 54 count bottle; all products purchased before May 2, 201950 bottlesClass II
F-1396-2019HoliCare Metabolism Cleansing (MET-CLS) tablets, 60 count bottle; lot # T8117104052 bottlesClass I
Based on the official FDA remedy

What to do — step by step

  1. Stop Using Now

    Immediately stop using the recalled capsules as they contain high lead levels that can cause lead poisoning.

How this recall unfolded

Recall timeline

FDA terminated this recall 2.8 years after the firm started it.

1. Firm started the recall: May 2, 201912. FDA classified it Class I: May 23, 201923. Published in FDA’s Enforcement Report: May 29, 201934. FDA terminated the recall: Feb 11, 2022420192022
  1. Firm started the recall
  2. FDA classified it Class I
  3. Published in FDA’s Enforcement Report
  4. FDA terminated the recall

Dates from the agency record only; steps without a date are left out.

Similar recalls

Latest food recalls

Keep exploring

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-1394-2019 (May 2, 2019) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-1394-2019 to see it in context.
  • Plain-language summary written by qwen3:4b on October 5, 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.
GovInfoNow is an independent guide. We are not FDA or any government agency. Always confirm details with the official recall.Data: CPSC · FDA · NHTSA · USDA