DG Health brand Sugar Free Daily Fiber in 10 oz. plastic containers (UPC: 860005934294).
Dollar General Corporation recalled this product and the FDA reported the enforcement action on 29 March 2023 as Class III. The recall was initiated by the firm. Product is missing warning declaration that it contains phenylalanine.
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
- DG Health brand Sugar Free Daily Fiber in 10 oz. plastic containers (UPC: 860005934294).
- UPC
- 860005934294
- Reason for recall
- Product is missing warning declaration that it contains phenylalanine.
- Recalling firm
- Dollar General Corporation
- Firm location
- Goodlettsville, Tennessee, United States
- Classification
- Class III
- Status
- Terminated
- Recall number
- F-0650-2023
- Quantity
- 89,136 units
- Distribution
- Products were distributed to the following states: AL, AZ, AR, CA, CO, CT, DE, FL, GA, ID, IL, IN, IA, KS, KY, LA, ME, MD, MA, MI, MN, MS, MO, NE, NV, NH, NJ, NM, NY, NC, ND, OH, OK, OR, PA, RI, SC, SD, TN, TX, UT, VT, VA, WA, WV, WI, & WY.
- Initiated
- 1 March 2023
- Reported by FDA
- 29 March 2023
- Terminated
- 18 August 2023
- Firm notified by
- Product codes
- Batch codes: GB10069, GB10070, GB10071, GB10073, GB10074, GB10075, GB10081, GB10082, GB10083, GB10084, GB10085, GB10086, GB10087, GB10093, GB10094, GB10095, GB10096, GB 10097, GB10098, GB10099, GB10100, GB10101, GB10102, GB10108, GB10109, GB10110, GB10111, and GB10125. Expiration Dates: Jun-24, Jul-24, and Aug-24
Reading this record
Five things about this record are not in the record itself, and each one changes how it should be read.
- Class III means the FDA judged that the product was unlikely to cause harm but violated FDA labelling or manufacturing regulation. 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 6 months, from 1 March 2023 to termination on 18 August 2023. 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 45 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: Arizona, Arkansas, California, Colorado, Connecticut, Delaware, Florida, Georgia, Idaho, Illinois, Indiana, Iowa, Kansas, Kentucky, Louisiana, Maine, Maryland, Massachusetts, Michigan, Minnesota, Mississippi, Missouri, Nebraska, Nevada, New Hampshire, New Jersey, New Mexico, New York, North Carolina, North Dakota, Ohio, Oklahoma, Oregon, Pennsylvania, Rhode Island, South Carolina, South Dakota, Tennessee, Texas, Utah, Vermont, Virginia, Washington, West Virginia, Wisconsin. Those pages count recalls by where the RECALLING FIRM sits, which is a different question from where this product went.
Other records from Dollar General Corporation
The FDA opens one enforcement record per product code, so several of these are frequently one recall event. 27 other records name this firm.
All 28 records for Dollar General Corporation
All 2023 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.