Skip to main content
CriticalFDAfda-F-1427-2014UNDECLARED ALLERGEN

DEL CAMPO PAPA SECA DRIED POTATO NET WT 14 OZ IMPORTED BY MEGABUSINESS PRODUCT OF PERU. UPC CODE 891726000218

⚠ 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
39
Recall Date
December 13, 2013
Issuing Agency
Hazard
Undeclared Allergen

FDA Recall Notice

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-1427-2014.

Undeclared sulfites.

Corrective Action (per FDA)

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-1427-2014.

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 Megabusiness Llc. 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-1427-2014.

MEGABUSINESS LLC.

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.

Visit FDA.gov →

📣 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.

How to report to FDAFile a report at FDA

Megabusiness Llc. Recall FAQ

Megabusiness Llc. is the subject of a food safety report: DEL CAMPO PAPA SECA DRIED POTATO NET WT 14 OZ IMPORTED BY MEGABUSINESS PRODUCT OF PERU. UPC CODE 891726000218. The notice was published on December 13, 2013 by the U.S. Food and Drug Administration (FDA). Approximately 39 units are potentially affected.