Skip to main content
High RiskFDAfda-F-1951-2012UNDECLARED ALLERGEN

Libby's Gourmet Desserts brand pecan pie. Pies placed in metal pie tins which are then put in a cardboard sleeve with plastic wrapping

Category
Units Affected
696
Recall Date
July 17, 2012
Issuing Agency
Hazard
Undeclared Allergen

FDA Recall Notice

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-1951-2012.

No ingredient Statement on box. Labeled incorrectly. Product is being recalled because there is no ingredient statement on the box. Product contains multiple allergen ingredients.

Corrective Action (per FDA)

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-1951-2012.

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 Libby's Gourmet Desserts 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-1951-2012.

Libby's Gourmet Desserts

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

Libby's Gourmet Desserts Recall FAQ

Libby's Gourmet Desserts is the subject of a food safety report: Libby's Gourmet Desserts brand pecan pie. Pies placed in metal pie tins which are then put in a cardboard sleeve with plastic wrapping. The notice was published on July 17, 2012 by the U.S. Food and Drug Administration (FDA). Approximately 696 units are potentially affected.