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CriticalFDAfda-F-1573-2016LISTERIA

Maytag Blue cheese crumbles re-packaged and sold in plastic containers with scale labels in various weights. Product was labeled as Mayt...

⚠ Critical Alert — Stop Using Immediately

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

Category
Units Affected
210
Recall Date
March 3, 2016
Issuing Agency
Hazard
Listeria

FDA Recall Notice

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-1573-2016.

Product may be contaminated with Listeria monocytogenes.

Corrective Action (per FDA)

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-1573-2016.

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 Hy-vee Stores Inc 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-1573-2016.

Hy-Vee Stores Inc

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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Hy-vee Stores Inc Recall FAQ

Hy-vee Stores Inc is the subject of a dairy safety report: Maytag Blue cheese crumbles re-packaged and sold in plastic containers with scale labels in various weights. Product was labeled as Mayt.... The notice was published on March 3, 2016 by the U.S. Food and Drug Administration (FDA). Approximately 210 units are potentially affected.