DG Health brand Sugar Free Daily Fiber in 10 oz. plastic containers (UPC: 860005934294).
Summary
The FDA issued a Class III for DG Health brand Sugar Free Daily Fiber in 10 oz. plastic containers (UPC: 860005 by Dollar General Corporation. Reason: Product is missing warning declaration that it contains phenylalanine..
Details
Source
Food Recall
External ID
F-0650-2023
Action Date
2023-03-29
Status
Terminated
Category
food
Product Description
DG Health brand Sugar Free Daily Fiber in 10 oz. plastic containers (UPC: 860005934294).
Lot/Code Info: 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
Quantity Affected: 89,136 units
Reason for Recall
Product is missing warning declaration that it contains phenylalanine.
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.
Type: Voluntary: Firm initiated
Recall Initiated: 2023-03-01
Company
Goodlettsville, TN
Context & Analysis
This is a Class III recall. Class III recalls involve products unlikely to cause adverse health consequences, but that violate FDA regulations.
This was one of 503 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Dollar General Corporation has 26 FDA actions in our database, including 26 recalls.
Frequently Asked Questions
What is a Class III recall?
A Class III recall involves products that are unlikely to cause adverse health effects but violate FDA labeling or manufacturing regulations.
What should I do if I have this product?
Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (Dollar General Corporation) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Dollar General Corporation have FDA actions?
Dollar General Corporation has 26 FDA actions in our database, including 26 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-0650-2023" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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