Lily s Peppermint Flavor Baking Chips, 7 oz. Pouch
LILY'S SWEETS LLC recalled this product and the FDA reported the enforcement action on 16 February 2022 as Class II. The recall was initiated by the firm. 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.

The record
Every field below is published by the FDA in the openFDA food enforcement database. Check the FDA notice before acting on any recall: this page is a reading of the public record, not a substitute for it.
- Product
- Lily s Peppermint Flavor Baking Chips, 7 oz. Pouch
- Reason for recall
- 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.
- Recalling firm
- LILY'S SWEETS LLC
- Firm location
- Boulder, Colorado, United States
- Classification
- Class II
- Status
- Terminated
- Recall number
- F-0739-2022
- Quantity
- 18,855 cases (49,494 lbs.)
- 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
- Initiated
- 13 January 2022
- Reported by FDA
- 16 February 2022
- Terminated
- 3 March 2022
- Firm notified by
- Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
- Product codes
- 01/24/2023 BS 01/25/2023 AS, 01/25/2023 BS, 01/25/23 CS 01/26/2023 AS, 01/26/2023 BS, 01/26/23 CS 01/27/2023 AS, 01/27/2023 BS, 01/27/23 CS 01/28/2023 AS, 01/28/2023 BS 01/31/2023 AS, 01/31/2023 BS 02/01/2023 AS, 02/01/2023 BS, 02/01/23 CS 02/02/2023 AS, 02/02/2023 BS, 02/02/23 CS 02/03/2023 AS, 02/03/2023 BS, 02/03/23 CS 02/04/2023 AS, 02/04/2023 BS
Reading this record
Five things about this record are not in the record itself, and each one changes how it should be read.
- Class II means the FDA judged a remote probability of serious harm, or a probability of temporary or medically reversible harm. The class is assigned by an agency health hazard evaluation under 21 CFR 7.41, not by the firm.
- The firm started this recall itself. Most FDA food recalls are voluntary, and a recall is a food safety plan working rather than failing. The circumstances in which the agency asks for one instead are set out in 21 CFR 7.45.
- This record is the only one the FDA opened for its recall event, so it covers a single product code.
- The recall ran for 7 weeks, from 13 January 2022 to termination on 3 March 2022. Termination means the agency judged that all reasonable effort had been made, under 21 CFR 7.55, and it says nothing about whether product remained in circulation.
- The distribution pattern names 21 states, and the FDA published the enforcement report 5 weeks after the firm began the recall.
- Recalls of a snack or confectionery product run a median of 7 months, so this one was shorter than usual for its category. Snacks and confectionery recall for allergens more than for anything else, because a chocolate or a coated snack passes through shared equipment carrying milk, soy and nuts, and the label is the only control between them and the consumer.
Named in the distribution pattern: Alabama, Arizona, California, Colorado, Florida, Georgia, Kentucky, Minnesota, Missouri, Mississippi, North Carolina, New Hampshire, New Mexico, Nevada, New York, Ohio, Pennsylvania, Texas, Utah, Virginia, Washington. Those pages count recalls by where the RECALLING FIRM sits, which is a different question from where this product went.
Filed under snacks and confectionery. A product can sit in more than one.
Other snacks and confectionery recalls
These are the closest records in the corpus: the same kind of food. Unlike the firm’s own records below, they come from different companies, which is what makes them a pattern rather than a history.
All 2022 recalls · All FDA food recall data
Behind every recall is a clause somebody has to produce evidence for at their next audit. Krolda maps supplier documents to the clause they satisfy in FSSC 22000, IFS Food and 21 CFR 117, and routes the corrective action when the evidence is missing.
Early accessRecall records come from the openFDA food enforcement API, published by the U.S. Food and Drug Administration in the public domain. Krolda adds the hazard classification and the clause mapping; neither is an FDA determination. Always check the FDA notice before acting on a recall.