PlainRecalls
FDA Food Verify with FDA Food → Moderate Class II Terminated

CELLECT brand and ESSENTIALS FACTOR Cell Synergy brand Unflavored Powdered Mix Multi-Mineral & Vitamin Supplement NET WT. Approximately 20.4 OZ (1.28 LB) 579g in white plastic bottles

Reported: November 13, 2019 Initiated: September 27, 2019 #F-0100-2020 3943 bottles units

Images Unlimited Products, dba Cellect Products issued this FDA Food recall on November 13, 2019. Classified as Moderate severity (Class II). Approximately 3943 bottles units are affected. The recall was issued because: Product contains unsafe levels of Arsenic and Lead. This recall notice is sourced from official FDA Food enforcement records. Below you will find the complete product description, hazard information, remedy instructions, and related recalls from the same manufacturer or product category.

Recall Insight

This FDA Food action (record #F-0100-2020) was formally reported on November 13, 2019, with the manufacturer initiating the action on September 27, 2019. It is classified under Moderate severity (Class II), with a current status of Terminated. Images Unlimited Products, dba Cellect Products is listed as the recalling firm, operating out of Port Jefferson Station, NY. Federal records indicate 3943 bottles units are affected.

The documented reason for this recall is: Product contains unsafe levels of Arsenic and Lead Distribution data in the federal record shows the product reached: 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, …. Distribution scope directly affects the consumer exposure window and determines whether a recall remains regional or escalates into a nationwide advisory.

To put this record in context, PlainRecalls indexes 83,949 recalls across the FDA, CPSC, NHTSA and USDA FSIS going back to 1995. Within the same product category, the database holds 6 closely related recalls. That clustering is a signal — repeated actions in a narrow category often indicate a systemic quality-control issue, a supplier-wide contamination, or a design defect that has propagated across product lines. This recall is roughly 7 years old; older recalls can remain relevant because many units enter resale, rental, and secondary-market channels where the original warning never reaches the end user. Always cross-check the recall number against the official agency page before relying on any summary.

Recall Distribution by Severity Class

Severity1Class I (Critical)Class II (Moderate)Class III (Low)
Recall Distribution by Severity Class

Severity

Moderate

Units Affected

3943 bottles

Related Recalls

6

0 from same agency

Product Description

CELLECT brand and ESSENTIALS FACTOR Cell Synergy brand Unflavored Powdered Mix Multi-Mineral & Vitamin Supplement NET WT. Approximately 20.4 OZ (1.28 LB) 579g in white plastic bottles

Reason for Recall

Product contains unsafe levels of Arsenic and Lead

Details

Units Affected
3943 bottles
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, Romania, Singapore, Switzerland and United Arab Emirates
Location
Port Jefferson Station, NY

Recall Profile

Structured summary of the FDA Food recall record
Attribute Value
Agency U.S. Food and Drug Administration
Severity class Moderate (Class II)
Status Terminated
Recall number F-0100-2020
Date reported November 13, 2019
Date initiated September 27, 2019
Recalling firm Images Unlimited Products, dba Cellect Products
Units affected 3943 bottles
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, Romani…

Profile values are sourced directly from the official FDA Food enforcement record. Source: U.S. Food and Drug Administration.

Scale of Impact

3943 bottles units affected — limited or regional distribution scale.

Regional (<10K units) ✓ This recall
Multi-state (10K – 100K units)
Large-scale (100K – 1M units)
Massive (≥1M units)

Bracket cutoffs follow federal recall-disclosure conventions; bar widths scale linearly within each bracket. Source: PlainRecalls analysis of U.S. Food and Drug Administration filings.

Frequently Asked Questions

What product was recalled?
CELLECT brand and ESSENTIALS FACTOR Cell Synergy brand Unflavored Powdered Mix Multi-Mineral & Vitamin Supplement NET WT. Approximately 20.4 OZ (1.28 LB) 579g in white plastic bottles. Recalled by Images Unlimited Products, dba Cellect Products. Units affected: 3943 bottles.
Why was this product recalled?
Product contains unsafe levels of Arsenic and Lead
Which agency issued this recall?
This recall was issued by the FDA Food on November 13, 2019. Severity: Moderate. Recall number: F-0100-2020.
Where was the recalled product distributed?
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, Romania, Singapore, Switzerland and United Arab Emirates.
How do I check if my product is affected by a recall?
Check the product description and recall number (F-0100-2020) against your product. Visit the official FDA Food website for the most current information. You can also use our Recall Checker tool to search by product name or brand.
What are the health risks of consuming a recalled food product?
Recalled food products may contain contaminants, undeclared allergens, or harmful bacteria such as Salmonella, Listeria, or E. coli. Consuming these products can cause foodborne illness ranging from mild gastrointestinal symptoms to serious conditions requiring hospitalization. If you have consumed a recalled food product and experience symptoms, contact your healthcare provider and report to the FDA via MedWatch.

Recall Context

Product recalls are issued when a manufacturer, distributor, or federal agency determines that a product poses a safety risk to consumers. This recall is classified as moderate severity, indicating the product may cause temporary or medically reversible health consequences. Across PlainRecalls, we track 83,000+ recalls from FDA, CPSC, and NHTSA to help consumers stay informed and act quickly when safety issues arise.

Nearby Recalls in This Category

Other recalls in the same product category — useful for spotting patterns across the same defect class or manufacturer.

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Data Sources

Data as of 2025. Source: FDA, CPSC, NHTSA, USDA FSIS federal recall databases.

  • Source: FDA — Food and Drug Administration, openFDA Enforcement API (food, drug, and medical device recalls)
  • Source: CPSC — Consumer Product Safety Commission Recalls API (consumer product recalls and hazards)
  • Source: NHTSA — National Highway Traffic Safety Administration Recalls API (vehicle safety recalls)
  • Source: USDA FSIS — Food Safety and Inspection Service (meat, poultry, and egg product recalls)

Recall information is sourced from official federal agency databases. Always verify recall details with the issuing agency for the most current status. This information is for research and awareness purposes only.

All federal data sources used on this page

Source: Federal recall agencies (FDA, CPSC, NHTSA, USDA FSIS) Aggregated multi-agency recall feeds · 2024 Recall data normalized across federal agency feeds; severity classifications follow each agency's own taxonomy (FDA Class I/II/III; CPSC, NHTSA, USDA FSIS).