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High RiskFDAfda-F-2926-2015UNDECLARED ALLERGEN

Vanilla bolis (tube), La Jalpita brand, 3.5 Fl oz., No UPC

Category
Units Affected
1,350
Recall Date
May 29, 2015
Issuing Agency
Hazard
Undeclared Allergen

FDA Recall Notice

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-2926-2015.

Vanilla bolis (tube) is recalled due to undeclared Yellow no. 6

Corrective Action (per FDA)

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-2926-2015.

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 Paleteria La Jalpita 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-2926-2015.

Paleteria La Jalpita

FDA

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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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Paleteria La Jalpita Recall FAQ

Paleteria La Jalpita is the subject of a food safety report: Vanilla bolis (tube), La Jalpita brand, 3.5 Fl oz., No UPC. The notice was published on May 29, 2015 by the U.S. Food and Drug Administration (FDA). Approximately 1,350 units are potentially affected.