UnratedFood recall · FDA · Published September 27, 2019
Cellect Unflavored Powdered Mix Recall: Unsafe Arsenic and Lead Levels
Cellect Unflavored Powdered Mix Multi-Mineral & Vitamin Supplement contains unsafe levels of arsenic and lead. Recalled products include white plastic bottles labeled 20.4 oz (579g) from May 2019.
“Cellect Unflavored Powdered Mix Recall: Unsafe Arsenic and Lead Levels.” GovInfoNow, updated October 5, 2026. https://govinfonow.com/recall/16591-cellect-unflavored-powdered-mix-recall-unsafe-arsenic-and-lead-levels. Based on FDA recall #F-0100-2020 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-0100-2020%22&limit=1).
The FDA announced on Sept. 27, 2019, that Images Unlimited Products dba Cellect Products voluntarily recalled CELLECT and ESSENTIALS FACTOR brand Unflavored Powdered Mix Multi-Mineral & Vitamin Supplement due to unsafe levels of arsenic and lead.
NET WT. Approximately 20.4 OZ (1.28 LB) 579g in white plastic bottles
Lot: 041907
MFG: 05/20/2019
The hazard
The product contains unsafe levels of arsenic and lead, according to the FDA.
Context
GovInfoNow's records show other recent recalls of similar products include Llorens Vitamin B-Complex Supplement Recall (2026-05-07) and U.S. Trading Company Dragonfly Thai Ginger Powder Recall (2026-05-15). Venzu Traders also issued a Cinnamon Powder Recall on 2025-11-14.
How to tell if you have this one
Check for white plastic bottles labeled 20.4 ounces (579g) with lot number 041907 manufactured on May 20, 2019.
Brand
Cellect
Category
Food
Based on the official FDA remedy
What to do — step by step
Stop Using It Now
Discard the recalled product immediately as it contains unsafe levels of arsenic and lead.
Where it went and when
Where it was distributed
Distributed nationwide, and outside the U.S.
Nationwide
Not listed
FDA distribution: “Product distributed nationwide in the US. Also sent to individual customers in Canada, United Kingdom, Australia, South Korea, Croatia, Hong Kong, India, Macau, Malaysia, Mexico, Netherlands, New Zealand, South Africa, Oman, Poland,…” 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 12 months after the firm started it.
1Firm started the recall
2FDA classified it Class II
3Published in FDA’s Enforcement Report
4FDA terminated the recall
Dates from the agency record only; steps without a date are left out.
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-0100-2020 (September 27, 2019) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-0100-2020 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.