Lily's Sweets LLC recalls 7 oz. Peppermint Baking Chips pouches due to soy lecithin presence. Consumers should check product dates and contact the company for details.
Lily s Sweets, LLC has initiated a recall of Lily s Peppermint Flavor Baking Chips , 7 oz. pouch, 6 pouches per case, corrugated case because the presence of soy lecithin.
Take action
Contact the company
📍Recalling firmLILY'S SWEETS LLC4840 Pearl East Cir Ste 201e · Boulder, CO 80301-6115
“Lily's Sweets Peppermint Baking Chips Recall: Soy Lecithin Present.” GovInfoNow, updated October 4, 2026. https://govinfonow.com/recall/13381-lily-s-sweets-peppermint-baking-chips-recall-soy-lecithin-present. Based on FDA recall #F-0739-2022 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-0739-2022%22&limit=1).
LILY'S SWEETS LLC recalled Lily's Peppermint Flavor Baking Chips, 7 oz. pouches because they contain soy lecithin, an undeclared allergen. The FDA announced the recall on Jan. 13, 2022. Owners should contact the company for a refund.
How to tell if you have it
Brand: Lily's Sweets
Product: Lily's Peppermint Flavor Baking Chips, 7 oz. Pouch
Lot codes: 01/24/2023 BS 01/25/2023 AS through 02/04/2023 BS
The hazard
The product contains soy lecithin, which is not listed on the label. This poses a risk to individuals with soy allergies.
Context
GovInfoNow's records show other recent recalls of similar products include JK Patisserie Chocolate Chip Cookie Recall (2026-09-04), ASUKAR TETAS Cherry Milkshake Popsicle Recall (2026-03-11), and Prospector Popcorn Recall (2026-04-28).
How to tell if you have this one
Check for 7 oz. pouches of Lily's Sweets Peppermint Flavor Baking Chips. The product was sold between January 24, 2023 and February 4, 2023.
Brand
Lily's Sweets
Category
Food
Based on the official FDA remedy
What to do — step by step
Check Product Dates
Look for the product's production and sale dates on the packaging, which range from January 24, 2023 to February 4, 2023.
Where it went and when
Where it was distributed
Distributed in 22 states.
Listed by the agency
Not listed
FDA distribution: “Product Distributed to the following States: IL, AL, AZ, CA, CO, FL,GA, KY, MN, MO, MS, NC, NH, NM, NV, NY, OH, PA, TX, UT, VA, WA” States read from FDA’s own wording; “not listed” means the notice does not name it.
States: Alabama, Arizona, California, Colorado, Florida, Georgia, Illinois, Kentucky, Minnesota, Mississippi, Missouri, Nevada, New Hampshire, New Mexico, New York, North Carolina, Ohio, Pennsylvania, Texas, Utah, Virginia, Washington.
Recall timeline
FDA terminated this recall 49 days after the firm started it.
1Firm started the recall
2Published in FDA’s Enforcement Report
3FDA classified it Class II
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-0739-2022 (January 13, 2022) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-0739-2022 to see it in context.
Plain-language summary written by qwen3:4b on October 4, 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.