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CriticalFDAfda-F-0771-2015LISTERIA

Red Apple W/ Cheese Net Wt: 5oz. (142g) Best If Enjoyed By: 12/06/14, DISTRIBUTED BY SHEETZ DISTRIBUTION SERVICES, LLC. CLAYSBURG, PA 166...

⚠ 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
48
Recall Date
December 9, 2014
Issuing Agency
Hazard
Listeria

FDA Recall Notice

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-0771-2015.

Possible contamination with Listeria monocytogenes.

Corrective Action (per FDA)

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-0771-2015.

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 Del Monte Fresh Produce Na, 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-0771-2015.

Del Monte Fresh Produce NA, 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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Del Monte Fresh Produce Na, Inc Recall FAQ

Del Monte Fresh Produce Na, Inc is the subject of a dairy safety report: Red Apple W/ Cheese Net Wt: 5oz. (142g) Best If Enjoyed By: 12/06/14, DISTRIBUTED BY SHEETZ DISTRIBUTION SERVICES, LLC. CLAYSBURG, PA 166.... The notice was published on December 9, 2014 by the U.S. Food and Drug Administration (FDA). Approximately 48 units are potentially affected.