Lower riskFood recall · FDA · Published November 4, 2015
Land O' Lakes Kozy Shack Indulgent Salted Caramel Pudding Recall: Egg Risk
Land O' Lakes recalls Kozy Shack Indulgent Salt: 31908941 lot may contain Vanilla Bean Pudding cups with egg. Consumers should check for egg content before use.
Kozy Shack is recalling one lot of Kozy Shack Indulgent Recipe Pudding in a Salted Caramel cardboard sleeve because it may contain Vanilla Bean Pudding cups, which contain egg.
Take action
Contact the company
📍Recalling firmLand O' Lakes, Inc4001 Lexington Ave N · Arden Hills, MN 55126-2934
“Land O' Lakes Kozy Shack Indulgent Salted Caramel Pudding Recall: Egg Risk.” GovInfoNow, updated August 18, 2026. https://govinfonow.com/recall/25776-land-o-lakes-kozy-shack-indulgent-salted-caramel-pudding-recall. Based on FDA recall #F-0322-2016 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-0322-2016%22&limit=1).
The FDA announced on November 4, 2015, that Land O'Lakes, Inc. is recalling one lot of Kozy Shack Indulgent Salted Caramel pudding because it may contain egg from Vanilla Bean Pudding cups. The recall involves 6,423 cases distributed across 18 states.
The product may contain Vanilla Bean Pudding cups, which contain egg. The FDA classified the recall as Class I.
Context
GovInfoNow's records show Land O'Lakes, Inc. has two other recalls on record since June 18, 2014. Other recent recalls of similar products include House of Flavors Vanilla Ice Cream Recall (February 26, 2026), Kerry KC Everyday Mac & Cheese Recall (July 29, 2026), and So Delicious Salted Caramel Cluster Cashewmilk Recall (December 15, 2025).
How to tell if you have this one
Check for the lot number 31908941 on the cardboard sleeve of Kozy Shack Indulgent Salted Caramel pudding. The product was sold in the United States.
Brand
Land O' Lakes
Category
Food
Based on the official FDA remedy
What to do — step by step
Check for Egg Content
If you have the recalled lot number 31908941, check if the pudding contains Vanilla Bean Pudding cups with egg.
Where it went and when
Where it was distributed
Distributed in 18 states.
Listed by the agency
Not listed
FDA distribution: “AZ, CA, CT, ID, MA, MD, ME, NC, NJ, NV, NY, OH, OR, PA, SC, UT, VA, and WA.” States read from FDA’s own wording; “not listed” means the notice does not name it.
States: Arizona, California, Connecticut, Idaho, Maine, Maryland, Massachusetts, Nevada, New Jersey, New York, North Carolina, Ohio, Oregon, Pennsylvania, South Carolina, Utah, Virginia, Washington.
Recall timeline
FDA terminated this recall 3 months after the firm started it.
1Firm started the recall
2FDA classified it Class I
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-0322-2016 (November 4, 2015) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-0322-2016 to see it in context.
Plain-language summary written by qwen3:4b on August 18, 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.