Eastland Food Corporation recalls Maesri Shrimp Powder due to unlisted FD&C Yellow #6, which may cause allergic reactions in some individuals. Consumers should check product codes and contact for details.
The New York Department of Agriculture and Markets notified Eastland Food Corp. that they analyzed a sample of the shrimp powder and determined that the product contained FD&C Yellow #6, but the label failed to declare its presence. Yellow #6 can cause an allergic reaction for a small population of individuals.
Eastland Food Corporation is recalling Maes:ri Shrimp Powder (6 oz) because it contains FD&C Yellow #6, an artificial dye not listed on the label. This dye can cause allergic reactions in a small number of people, so affected consumers should stop using it.
The shrimp powder contains FD&C Yellow #6, an artificial dye that is not declared on the label. This dye can cause allergic reactions in a small population of individuals, though the risk is low for most people.
People who own or use Maesri Shrimp Powder (6 oz) from Eastland Food Corporation are most at risk if they have an allergy to FD&C Yellow #6.
Check for the product code 210240 on the Maesri Shrimp Powder (6 oz) label. The recall applies to this specific product from Eastland Food Corporation.
Look for the product code 210240 on the Maesri Shrimp Powder (6 oz) label.
The product contains FD&C Yellow #6, which may cause allergic reactions in some people, so it is not safe for those with allergies.
Check for the product code 210240 on the Maesri Shrimp Powder (6 oz) label.
The recall does not specify a remedy, so contact Eastland Food Corporation for further instructions.
We’ve drafted a message you can send Eastland Food Corporation to request your refund or repair — edit it as you like.
Subject: Recall F-0724-2016 — Eastland Food Corporation Eastland Food Corporation Hello, I own a Eastland Food Corporation that is covered by recall F-0724-2016 from Eastland Food Corporation. 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.