RECALL RECORD — CLASS IIRecall closedF-0100-2020/FDA enforcement

Cellect Brand and Essentials Factor Cell Synergy Brand Unflavored Powdered Mix Multi-mineral &…

What you need to know

Class II
  • What happened

    Product contains unsafe levels of Arsenic and Lead

  • Health risk

    The product may cause temporary or medically reversible health consequences, or the probability of serious harm is remote. Lead is a toxic heavy metal with no safe blood lead level in children.

  • Action required

    Stop taking the supplement. Check the lot and UPC codes below, then return it to the retailer or contact the manufacturer about a refund. Seek medical advice if you have concerns about exposure.

Recall closed · classified by the FDANationwide (US)More supplements

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Product identification

Source: FDA FOOD

Brand nameImages Unlimited Products, Dba Cellect Products
Recalling firmImages Unlimited Products, Dba Cellect ProductsPort Jefferson Station, NY, United States
UPC / barcodesNo UPC listed in the FDA enforcement record.
Lot / date codes
  • Lot: 041907 MFG: 05/20/2019
Distribution area
Nationwide

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, Romania, Singapore, Switzerland and United Arab Emirates

United States, Canada, Mexico, United Kingdom, Australia

Quantity affected3943 bottles
Recall initiationFDA report date: November 13, 2019
FDA recall numberF-0100-2020

Beyond the headline

The recall, in context

Images Unlimited Products, Dba Cellect Products initiated this supplements recall on September 27, 2019. The FDA enforcement report states: Product contains unsafe levels of Arsenic and Lead. The FDA report lists distribution as: 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, Romania, Singapore, Switzerland and United Arab Emirates.

The FDA enforcement report describes the reason as: Product contains unsafe levels of Arsenic and Lead

Cellect Brand and Essentials Factor Cell Synergy Brand Unflavored Powdered Mix Multi-mineral &… was made or distributed by Images Unlimited Products, Dba Cellect Products in Port Jefferson Station, NY, United States. This page reflects FDA report F-0100-2020, dated November 13, 2019.

Why this is a Class II recall

Class II means the product may cause temporary or medically reversible health consequences, or the probability of serious harm is remote. In this recall, lead is a toxic heavy metal with no safe blood lead level in children.

FDA definition

The product may cause temporary or medically reversible health consequences, or the probability of serious harm is remote.

What to do now

  1. 1

    Stop using it

    Do not eat, drink or take the affected product.

  2. 2

    Check the codes

    Compare the lot and date codes against the table above.

  3. 3

    Return or discard

    Contact the retailer or recalling firm about a refund, and dispose of the product safely.

Consumer safety guide

Lead contamination

Possible health effects

Lead can affect the nervous system and is especially harmful to children and pregnant people. Symptoms may include abdominal pain, constipation, fatigue or headaches, but some exposed people have no obvious symptoms.

When symptoms may appear

Health effects depend on the amount and duration of exposure; there is no safe blood lead level in children.

Higher-risk groups

Infants, young children, pregnant people and anyone with repeated exposure are at greatest risk.

What to do now

  1. 1Stop using or eating the affected product and prevent children from handling it.
  2. 2Keep the packaging and ask the retailer or manufacturer about a refund; follow local guidance for safe disposal.
  3. 3If a child or pregnant person may have been exposed, contact a healthcare professional about blood lead testing.

Do not use home remedies or ignore possible exposure; clinical testing is the appropriate next step.

This is general consumer safety information, not medical advice or a diagnosis. Follow the official recall notice and contact a healthcare professional if you have concerns about exposure or symptoms.

Frequently asked

Questions about this recall

What is the Cellect Brand and Essentials Factor Cell Synergy Brand Unflavored Powdered Mix Multi-mineral &… recall?

Images Unlimited Products, Dba Cellect Products recalled Cellect Brand and Essentials Factor Cell Synergy Brand Unflavored Powdered Mix Multi-mineral &… in an FDA Class II enforcement action reported as F-0100-2020. Product contains unsafe levels of Arsenic and Lead

What should I do if I bought this product?

Stop taking the supplement. Check the lot and UPC codes below, then return it to the retailer or contact the manufacturer about a refund. Seek medical advice if you have concerns about exposure. Stop using or eating the affected product and prevent children from handling it. Keep the packaging and ask the retailer or manufacturer about a refund; follow local guidance for safe disposal. If a child or pregnant person may have been exposed, contact a healthcare professional about blood lead testing.

Is the Images Unlimited Products, Dba Cellect Products recall still active?

The FDA lists this recall as recall closed. It remains relevant if you still have the affected product or need to identify a historical recall.

Where can I verify this recall?

This page is normalized from the openFDA enforcement record F-0100-2020. You can verify it directly using the official source link on this page. VerifyRecall updates its index from public FDA enforcement data and does not replace advice from the FDA, the recalling firm or a healthcare professional.

Verify before you act.

VerifyRecall is independent and not affiliated with the FDA. Always confirm the latest status on the official source record.

Official source

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Record last synced from official openFDA enforcement data on November 14, 2026. Source record: official FDA notice.