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CriticalFDAfda-F-0559-2018UNDECLARED ALLERGEN

New Seasons Market Grab and Go Pre-Packaged Macaroni and Cheese - refrigerated. Product is packaged in aluminum shallow containers with ...

⚠ Critical Alert — Stop Using Immediately

This product has been flagged with severe risks (undeclared allergen). Stop using it now and contact the brand or FDA for a refund, repair, or replacement.

Category
Units Affected
924
Recall Date
December 28, 2017
Issuing Agency
Hazard
Undeclared Allergen

FDA Recall Notice

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-0559-2018.

New Seasons Market Grab and Go Pre-Packaged Macaroni and Cheese is recalled due to undeclared egg.

Corrective Action (per FDA)

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-0559-2018.

Recall terminated by FDA.

✅ What you should do

  1. Stop using the product if you own it.
  2. Check the model number, lot code, or sell-by date against the recall notice above.
  3. Contact New Seasons Market or the retailer where you bought it for a refund, replacement, or repair.
  4. For the most current official instructions, visit the FDA recall page.
  5. If you've been hurt by this product, report the incident to FDA.

Consumer Contact (per FDA)

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-0559-2018.

NEW SEASONS MARKET

FDA

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The FDA regulates drugs, medical devices, food, cosmetics, and tobacco. Adverse event reports and recall notices are the main public safety signal.

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📣 Report a food, supplement, or cosmetic problem to the FDA

If you had a reaction, found contamination, or experienced a labeling problem with this product, report it to the FDA. The agency uses consumer reports to track emerging safety signals and trigger recalls.

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New Seasons Market Recall FAQ

New Seasons Market is the subject of a dairy safety report: New Seasons Market Grab and Go Pre-Packaged Macaroni and Cheese - refrigerated. Product is packaged in aluminum shallow containers with .... The notice was published on December 28, 2017 by the U.S. Food and Drug Administration (FDA). Approximately 924 units are potentially affected.