Skip to main content
CriticalFDAfda-F-2204-2017UNDECLARED ALLERGEN

7-ELEVEN CAESAR SIDE SALAD 3 oz. packaged in clear plastic container

⚠ 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
740
Recall Date
April 13, 2017
Issuing Agency
Hazard
Undeclared Allergen

FDA Recall Notice

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-2204-2017.

Undeclared milk, eggs, wheat and fish (anchovies).

Corrective Action (per FDA)

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-2204-2017.

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 Del Monte Fresh Produce N.a., Inc. Hq 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-2204-2017.

Del Monte Fresh Produce N.A., Inc. HQ

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

Del Monte Fresh Produce N.a., Inc. Hq Recall FAQ

Del Monte Fresh Produce N.a., Inc. Hq is the subject of a produce safety report: 7-ELEVEN CAESAR SIDE SALAD 3 oz. packaged in clear plastic container. The notice was published on April 13, 2017 by the U.S. Food and Drug Administration (FDA). Approximately 740 units are potentially affected.