KPCM New York Inc. recalls Preema Bright Red and Orange Food Color Powders due to banned color additives and potential effects on children's attention and activity levels. Check product labels for EAN codes and batch numbers.
Products contain banned color, carmoisine and undeclared FD&C Yellow 5 and FD&C Red 40
KPCM New York Inc. is recalling Preema brand food color powders because they contain banned colorants and undeclared food dyes that may affect children's attention and activity. These products are sold in small plastic bottles with specific batch numbers and expiration dates.
These food color powders contain carmoisine and undeclared FD&C dyes that are banned in food products. The dyes may cause adverse effects on children's attention and activity levels, but the risk is not life-threatening.
Parents and caregivers of children who use these food color powders in products like snacks or drinks. Children with sensitivity to certain dyes may be at higher risk.
Check for Preema brand food color powders in small plastic bottles labeled with EAN codes 5021507271194 (Bright Red) or 5021507999463 (Orange). Products were sold with batch numbers 3757 (Bright Red) or 3902 (Orange) until May 2027.
Look for EAN codes 5021507271194 or 5021507999463 on the packaging to identify recalled items.
The products contain banned colorants and undeclared food dyes that may affect children's attention and activity levels.
The recall focuses on potential effects on children's attention and activity, but adults are not specifically mentioned as being at risk.
Check for Preema brand food color powders with EAN codes 5021507271194 (Bright Red) or 5021507999463 (Orange) and batch numbers 3757 or 3902.
We’ve drafted a message you can send Preema to request your refund or repair — edit it as you like.
Subject: Recall H-0490-2026 — Preema Preema Hello, I own a Preema that is covered by recall H-0490-2026 from Preema. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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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.
