“Sara Lee Pumpkin Spice Latte Pie Recall: Undeclared Red 40 Food Dye.” GovInfoNow, updated October 5, 2026. https://govinfonow.com/recall/16259-sara-lee-pumpkin-spice-latte-pie-recall-undeclared-red-40. Based on FDA recall #F-0448-2020 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-0448-2020%22&limit=1).
The Food and Drug Administration announced on Nov. 15, 2019, that Sara Lee Frozen Foods voluntarily recalled Chef Pierre Pumpkin Spice Latte Pie due to undeclared FD & C Red 40. The agency issued recall number F-0448-2020 for the frozen product distributed in several states.
How to tell if you have it
Brand: Sara Lee
Product: Chef Pierre 37 Ounce Pumpkin Spice Latte Pie, in foil pie pan with dome lid, frozen, 4 pies per wholesale case
SKU: 09368
UPC: 032100093682
Lot Codes: 0305273910, 0305273920, 0305283920
The hazard
The recall involves undeclared FD & C Red 40 in the Chef Pierre Pumpkin Spice Latte Pie. The FDA classified this as a Class III recall.
Context
GovInfoNow's records show Sara Lee Frozen Foods has one other recall on record since May 7, 2021, specifically a potential undeclared peanut hazard in Pecan Pie. Other recent recalls of similar products include Estrella Passion Fruit Drink Recall (May 19, 2026), Loard's Peppermint Ice Cream Recall (April 15, 2026), and Tiffany Food Corp Hexing Haw Balls Candy Recall (Aug. 28, 2026).
How to tell if you have this one
Check for the SKU number 09368 and UPC number 032100093682 on the packaging. The lot codes 0305273910, 0305273920, and 0305283920 are also associated with this recall.
Brand
Sara Lee
Product
Chef Pierre 37 Ounce Pumpkin Spice Latte Pie, in foil pie pan with dome lid, frozen, 4 pies per wholesale case, with
Category
Food
Based on the official FDA remedy
What to do — step by step
Check Product Details
Look for SKU number 09368 and UPC number 032100093682 on the packaging.
Where it went and when
Where it was distributed
Distributed in 16 states.
Listed by the agency
Not listed
FDA distribution: “TX, NM, OK, FL, SC, PA, VA, NY, MD, WI, KS, MO, MN, IA, NE, IL” States read from FDA’s own wording; “not listed” means the notice does not name it.
States: Florida, Illinois, Iowa, Kansas, Maryland, Minnesota, Missouri, Nebraska, New Mexico, New York, Oklahoma, Pennsylvania, South Carolina, Texas, Virginia, Wisconsin.
Recall timeline
FDA terminated this recall 12 months after the firm started it.
1Firm started the recall
2FDA classified it Class III
3Published in FDA’s Enforcement Report
4FDA terminated the recall
Dates from the agency record only; steps without a date are left out.
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
Official source: FDA Recall #F-0448-2020 (November 15, 2019) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-0448-2020 to see it in context.
Plain-language summary written by qwen3:4b on October 5, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.