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CriticalFDAfda-F-0389-2018LISTERIA

Casa Sanchez Foods, Real Guacamole; Net Wt. 9 oz.. (255 g), 1/2 gallon UPC: 0 78732 00412 2; 78732 00431-3 ; 0-78732-00412-2 Ingr...

⚠ 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
114,924
Recall Date
November 15, 2017
Issuing Agency
Hazard
Listeria

FDA Recall Notice

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-0389-2018.

FDA found Listeria monocytogenes in surveillance sample of guacamole.

Corrective Action (per FDA)

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-0389-2018.

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 Fante, Inc., Dba Casa Sanchez Foods 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-0389-2018.

FANTE, Inc., dba Casa Sanchez Foods

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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Fante, Inc., Dba Casa Sanchez Foods Recall FAQ

Fante, Inc., Dba Casa Sanchez Foods is the subject of a beverages safety report: Casa Sanchez Foods, Real Guacamole; Net Wt. 9 oz.. (255 g), 1/2 gallon UPC: 0 78732 00412 2; 78732 00431-3 ; 0-78732-00412-2 Ingr.... The notice was published on November 15, 2017 by the U.S. Food and Drug Administration (FDA). Approximately 114,924 units are potentially affected.