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CriticalFDAfda-F-0134-2021UNDECLARED ALLERGEN

Chicken Breast Chef Plate with Mac & Cheese and Broccoli, packaged in clear plastic container with printed label product code begins 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
580
Recall Date
October 27, 2020
Issuing Agency
Hazard
Undeclared Allergen

FDA Recall Notice

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-0134-2021.

Potential to contain undeclared egg

Corrective Action (per FDA)

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-0134-2021.

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 Whole Foods 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-0134-2021.

Whole Foods 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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Whole Foods Market Recall FAQ

Whole Foods Market is the subject of a dairy safety report: Chicken Breast Chef Plate with Mac & Cheese and Broccoli, packaged in clear plastic container with printed label product code begins with.... The notice was published on October 27, 2020 by the U.S. Food and Drug Administration (FDA). Approximately 580 units are potentially affected.