Mangalm LLC recalls Tops Strawberry Jam with unapproved color (carmoisine) due to potential health risks. Consumers should check product details and contact Mangalm for guidance.
Unapproved color (carmoisine).
Mangalm LLC is recalling Tops Strawberry Jam because it contains an unapproved color additive (carmoisine) that may pose health risks. This recall affects products sold in the U.S. with specific batch numbers and dates.
The jam contains carmoisine, a food coloring not approved for use in the U.S. This unapproved color could lead to health issues, particularly for individuals with sensitivities to it.
Consumers who purchased Tops Strawberry Jam from Mangalm LLC in the U.S. between the specified dates are affected. Those with allergies to carmoisine or related ingredients may be at higher risk.
Check for the UPC 8 904288 626322 and batch number 4F1101 on the product label. The jam was manufactured in India and distributed by Mangalm LLC in the U.S. until June 10, 2026.
Look for the UPC 8 904288 626322 and batch number 4F1101 on the jam label.
The recall is due to an unapproved color (carmoisine) that may pose health risks, but the product is not unsafe to eat if you do not have sensitivities to carmoisine.
The recall record does not specify a refund or replacement process; contact Mangalm LLC at info@mangalm.com for guidance.
Check the product label for the UPC and batch number. If you have the recalled product, contact Mangalm LLC for further instructions.
We’ve drafted a message you can send Mangalm to request your refund or repair — edit it as you like.
Subject: Recall H-0386-2026 — Mangalm Mangalm Hello, I own a Mangalm that is covered by recall H-0386-2026 from Mangalm. 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.