Food Colour Powder Recall: Preema Bright Red and Orange
FDA is recalling Preema brand Bright Red Food Colour Powder and Preema brand Orange Food Colour Powder from KPCM New York Inc. The products contain banned colors Carmoisine (E122) and Tartrazine (E102) and undeclared FD&C Yellow 5 and Red 40. A total of 720 bottles were distributed in New York and Massachusetts and the recall is rated moderate.
| Brand | KPCM New York Inc. |
|---|---|
| Product | 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 | Products contain banned color, carmoisine and undeclared FD&C Yellow 5 and FD&C Red 40 |
| Severity | moderate |
| Units affected | 720 |
| Distribution | NY, MA |
| Agency | FDA |
WHAT YOU SHOULD DO
- Stop using the recalled Preema Colour Powders immediately.
- Dispose of any remaining powder or return it to the place of purchase for a refund or replacement.
- Check packaging for batch numbers and best-before dates to determine if your product is affected (EANs 5021507271194 with Batch 3757, best before 05/2027; EAN 5021507999463 with Batch 3902, best before 08/2027).
- If you have experienced adverse effects, consult a health professional and report the incident to the FDA.
How to identify the recalled item
| Lot / date codes | a.) EAN: 5021507271194; Batch No.: 3757; Best before 05/2027 b.) EAN: 5021507999463; Batch No.: 3902; Best before 08/2027 |
|---|---|
| Lot / date codes | a.) EAN: 5021507271194; Batch No.: 3757; Best before 05/2027 b.) EAN: 5021507999463; Batch No.: 3902; Best before 08/2027 |
These are the identifiers FDA published for this recall. Most recall notices list no UPC or model number at all — if the code on your item is not shown here, that does not mean the item is excluded. Check the official notice, or contact the company.
This is an automatically maintained record of an official recall notice. Details can change; always follow the official notice linked above. See all records in the Recall Database.