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CriticalFDAfda-F-1583-2016LISTERIA

Pita Pal Mediterranean Three Bean Net Wt. 8 oz. (226g) UPC: 8-50157-0007-7 Keep Refrigerated Pita Pal Foods, LP Houston, TX 7003 www.pita...

⚠ 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
560
Recall Date
May 5, 2016
Issuing Agency
Hazard
Listeria

FDA Recall Notice

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-1583-2016.

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-1583-2016.

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 Pita Pal Foods Lp 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-1583-2016.

Pita Pal Foods LP

FDA

About the U.S. Food and Drug Administration

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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Pita Pal Foods Lp Recall FAQ

Pita Pal Foods Lp is the subject of a produce safety report: Pita Pal Mediterranean Three Bean Net Wt. 8 oz. (226g) UPC: 8-50157-0007-7 Keep Refrigerated Pita Pal Foods, LP Houston, TX 7003 www.pita.... The notice was published on May 5, 2016 by the U.S. Food and Drug Administration (FDA). Approximately 560 units are potentially affected.