Skip to main content
CriticalFDAfda-F-1892-2013UNDECLARED ALLERGEN

Olde Cape Cod Chipotle Ranch dressing, 16 oz. Item Number: 90997-11630

⚠ 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.

Units Affected
2,273
Recall Date
September 5, 2013
Issuing Agency
Hazard
Undeclared Allergen

FDA Recall Notice

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-1892-2013.

Product may be labeled with an incorrect back panel label that does not declare the allergens milk and egg.

Corrective Action (per FDA)

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-1892-2013.

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 Cains Foods L.p. 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-1892-2013.

Cains Foods L.P.

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

Cains Foods L.p. Recall FAQ

Cains Foods L.p. is the subject of a snacks & candy safety report: Olde Cape Cod Chipotle Ranch dressing, 16 oz. Item Number: 90997-11630. The notice was published on September 5, 2013 by the U.S. Food and Drug Administration (FDA). Approximately 2,273 units are potentially affected.