Home Alone International Delight Peppermint Mocha Zero Sugar, 32oz plastic bottle, 6…
DANONE US LLC recalled this product and the FDA reported the enforcement action on 6 November 2024 as Class II. The recall was initiated by the firm. The International Delight Zero Sugar Peppermint Mocha is recalled because it was mis-labeled as zero sugar but it contains sugar.
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
- Home Alone International Delight Peppermint Mocha Zero Sugar, 32oz plastic bottle, 6 bottles per case. Refrigerated.
- Reason for recall
- The International Delight Zero Sugar Peppermint Mocha is recalled because it was mis-labeled as zero sugar but it contains sugar.
- Recalling firm
- DANONE US LLC
- Firm location
- Broomfield, Colorado, United States
- Classification
- Class II
- Status
- Terminated
- Recall number
- F-0070-2025
- Quantity
- 1799 cases
- Distribution
- Distributed directly in IA, IN, TN, and TX. Product was further distributed in AR, GA, IL, IN, IA, KY, MS, NM, NE, OK, TN, TX, and WI.
- Initiated
- 12 October 2024
- Reported by FDA
- 6 November 2024
- Terminated
- 12 February 2025
- Firm notified by
- Product codes
- BEST BY 02.25.25
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 4 months, from 12 October 2024 to termination on 12 February 2025. 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 12 states, and the FDA published the enforcement report 4 weeks after the firm began the recall.
- The product description on this record names no food this site can classify, so it appears on no food-type page. That is a limit of the description rather than of the recall.
Named in the distribution pattern: Indiana, Tennessee, Georgia, Illinois, Iowa, Kentucky, Mississippi, New Mexico, Nebraska, Oklahoma, Texas, Wisconsin. Those pages count recalls by where the RECALLING FIRM sits, which is a different question from where this product went.
Other records from DANONE US LLC
The FDA opens one enforcement record per product code, so several of these are frequently one recall event. 15 other records name this firm.
All 16 records for DANONE US LLC
All 2024 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.