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

a.) Preema brand Bright Red Food Colour Powder; Net Weight .88oz/25gm; packaged in small plastic bottle; INGREDIENTS: SODIUM CHLORIDE, COLOUR (TARTRAZINE, CARMOSINE, ALLURA RED) CHECK THE LEGAL LIMIT, CONTAINS NO ANIMAL MATTER. E102, E122, E129 may have an adverse effect on activity and attention in children b.) Preema brand Orange Food Colour Powder; Net Weight .88oz/25gm; packaged in a small plastic bottle; INGREDIENTS: SODIUM CHLORIDE, COLOUR (TARTRAZINE, CARMOSINE, ALLURA RED) CHECK THE LEG

Reported: February 18, 2026 Initiated: January 29, 2026 #H-0490-2026 720 bottles units

KPCM New York Inc. issued this FDA Food recall on February 18, 2026. Classified as Moderate severity (Class II). Approximately 720 bottles units are affected. The recall was issued because: Products contain banned color, carmoisine and undeclared FD&C Yellow 5 and FD&C Red 40. 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 #H-0490-2026) was formally reported on February 18, 2026, with the manufacturer initiating the action on January 29, 2026. It is classified under Moderate severity (Class II), with a current status of Ongoing. KPCM New York Inc. is listed as the recalling firm, operating out of Maspeth, NY. Federal records indicate 720 bottles units are affected.

The documented reason for this recall is: Products contain banned color, carmoisine and undeclared FD&C Yellow 5 and FD&C Red 40 Distribution data in the federal record shows the product reached: NY, MA. 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, of which 6 were also issued by FDA Food. 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. Because this recall is recent, remedy windows and replacement inventory are most likely still actively available from the firm or retailer. 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

720 bottles

Related Recalls

6

6 from same agency

Product Description

a.) Preema brand Bright Red Food Colour Powder; Net Weight .88oz/25gm; packaged in small plastic bottle; INGREDIENTS: SODIUM CHLORIDE, COLOUR (TARTRAZINE, CARMOSINE, ALLURA RED) CHECK THE LEGAL LIMIT, CONTAINS NO ANIMAL MATTER. E102, E122, E129 may have an adverse effect on activity and attention in children b.) Preema brand Orange Food Colour Powder; Net Weight .88oz/25gm; packaged in a small plastic bottle; INGREDIENTS: SODIUM CHLORIDE, COLOUR (TARTRAZINE, CARMOSINE, ALLURA RED) CHECK THE LEGAL LIMIT, CONTAINS NO ANIMAL MATTER. E102, E122, E129 may have an adverse effect on activity and attention in children

Reason for Recall

Products contain banned color, carmoisine and undeclared FD&C Yellow 5 and FD&C Red 40

Details

Recalling Firm
KPCM New York Inc.
Units Affected
720 bottles
Distribution
NY, MA
Location
Maspeth, 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 Ongoing
Recall number H-0490-2026
Date reported February 18, 2026
Date initiated January 29, 2026
Recalling firm KPCM New York Inc.
Units affected 720 bottles
Distribution NY, MA

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

Scale of Impact

720 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?
a.) Preema brand Bright Red Food Colour Powder; Net Weight .88oz/25gm; packaged in small plastic bottle; INGREDIENTS: SODIUM CHLORIDE, COLOUR (TARTRAZINE, CARMOSINE, ALLURA RED) CHECK THE LEGAL LIMIT, CONTAINS NO ANIMAL MATTER. E102, E122, E129 may have an adverse effect on activity and attention in children b.) Preema brand Orange Food Colour Powder; Net Weight .88oz/25gm; packaged in a small plastic bottle; INGREDIENTS: SODIUM CHLORIDE, COLOUR (TARTRAZINE, CARMOSINE, ALLURA RED) CHECK THE LEGAL LIMIT, CONTAINS NO ANIMAL MATTER. E102, E122, E129 may have an adverse effect on activity and attention in children. Recalled by KPCM New York Inc.. Units affected: 720 bottles.
Why was this product recalled?
Products contain banned color, carmoisine and undeclared FD&C Yellow 5 and FD&C Red 40
Which agency issued this recall?
This recall was issued by the FDA Food on February 18, 2026. Severity: Moderate. Recall number: H-0490-2026.
Where was the recalled product distributed?
Distribution: NY, MA.
How do I check if my product is affected by a recall?
Check the product description and recall number (H-0490-2026) 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).