a.) Preema brand Bright Red Food Colour Powder recall
Recalled by KPCM New York Inc.
The product, as the FDA describes it: 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
Why it was recalled
Products contain banned color, carmoisine and undeclared FD&C Yellow 5 and FD&C Red 40
What to do if you have it
This is a labelling failure rather than spoiled food, so it matters entirely to whoever eats it. If nobody in your household reacts to what went undeclared here, the product is not dangerous to you, though you can still return it. If somebody does, treat every package from the affected run as unsafe no matter how much has already been eaten without incident.
How to tell whether your package is one of them
A recall covers particular production runs, not everything the company makes, so the codes decide it. These are the ones the FDA published. Match them against what is printed on your package, usually near the best-before date.
a.) EAN: 5021507271194; Batch No.: 3757; Best before 05/2027 b.) EAN: 5021507999463; Batch No.: 3902; Best before 08/2027
The details on record
| Recalling company | KPCM New York Inc. |
|---|---|
| Company location | Maspeth, NY |
| Where it was distributed | NY, MA |
| How much was recalled | 720 bottles |
| Recall started | January 29, 2026 |
| Published by the FDA | February 18, 2026 |
| Recall type | Voluntary: Firm initiated |
| How the company announced it | Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit |
| FDA recall number | H-0490-2026 |
Everything above comes from the FDA enforcement report for this recall. Read the official notice for the company's own wording, contact numbers, and any photographs of the packaging.
The other half of the answer
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