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CriticalFDAfda-F-1602-2015UNDECLARED ALLERGEN

8 in. sundried tomato flavored tortilla wraps, packaged in re-sealable polypropylene bags, 10 wraps per bag. Sold under the El Popocatepe...

⚠ 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
55
Recall Date
February 20, 2015
Issuing Agency
Hazard
Undeclared Allergen

FDA Recall Notice

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-1602-2015.

El Popocatepetl Ind., Inc. of Chicago, Illinois is voluntarily recalling El Popocatepetl's 8 in. Chipotle, Spinach Pesto, and Sun Dried Tomato Wraps because they may contain undeclared milk and Yellow No. 5.

Corrective Action (per FDA)

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-1602-2015.

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 El Popocatepetl Ind., 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-1602-2015.

El Popocatepetl Ind., Inc.

FDA

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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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El Popocatepetl Ind., Inc. Recall FAQ

El Popocatepetl Ind., Inc. is the subject of a produce safety report: 8 in. sundried tomato flavored tortilla wraps, packaged in re-sealable polypropylene bags, 10 wraps per bag. Sold under the El Popocatepe.... The notice was published on February 20, 2015 by the U.S. Food and Drug Administration (FDA). Approximately 55 units are potentially affected.