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Dollar General Corporation Recall: Product is missing warning declaration that it contains phenylalanine.

United States

TerminatedClass III

Company
Dollar General Corporation
Product
DG Health brand Sugar Free Daily Fiber in 10 oz. plastic con…
Recall date
March 1, 2023
Terminated
August 18, 2023
Source
FDA

Reason for recall

Product is missing warning declaration that it contains phenylalanine.

  1. - Recall initiated
  2. - Reported by source
  3. - Recall terminated
Recalled products
Product description UPC Quantity Lot / code information
DG Health brand Sugar Free Daily Fiber in 10 oz. plastic containers (UPC: 860005934294). 860005934294 89,136 units 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

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.

Official source record

Agency
FDA
Dataset
FDA Food Enforcement (Recalls)
Recall number
F-0650-2023
Event ID
91809
Status
Terminated
Classification
Class III
Company
Dollar General Corporation
Product description
DG Health brand Sugar Free Daily Fiber in 10 oz. plastic containers (UPC: 860005934294).
Quantity
89,136 units
Reason
Product is missing warning declaration that it contains phenylalanine.
Recall initiation date
March 1, 2023
Report date
March 29, 2023
Classification date
Not published in this source record
Termination date
August 18, 2023
Distribution pattern
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.
UPC, lot, and code information
UPC 860005934294; 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
Voluntary or mandated
Voluntary: Firm initiated
Initial notification method
E-Mail
Source last updated
Not tracked separately from the Public Health Trace retrieval date below
Public Health Trace retrieval date

Responsible company: Dollar General Corporation

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Distribution map

A map highlighting the states named in the source's distribution description.

Shading reflects state-level totals only, as published by the source. It does not imply county-level or point-level precision.

Distribution map
State Distributed
Alabama 1
Arizona 1
Arkansas 1
California 1
Colorado 1
Connecticut 1
Delaware 1
Florida 1
Georgia 1
Idaho 1
Illinois 1
Indiana 1
Iowa 1
Kansas 1
Kentucky 1
Louisiana 1
Maine 1
Maryland 1
Massachusetts 1
Michigan 1
Minnesota 1
Mississippi 1
Missouri 1
Nebraska 1
Nevada 1
New Hampshire 1
New Jersey 1
New Mexico 1
New York 1
North Carolina 1
North Dakota 1
Ohio 1
Oklahoma 1
Oregon 1
Pennsylvania 1
Rhode Island 1
South Carolina 1
South Dakota 1
Tennessee 1
Texas 1
Utah 1
Vermont 1
Virginia 1
Washington 1
West Virginia 1
Wisconsin 1
Wyoming 1

States shown are extracted from the source's free-text distribution description above; a narrative description (e.g. "distributed nationwide") may not list individual states to extract.

Where this information comes from

View FDA enforcement record -- the specific openFDA record this summary was built from.

No separate FDA public notice was found for this enforcement record. The information below comes from FDA's Recall Enterprise System through openFDA.

FDA Enforcement Reports -- FDA's general, official recall and enforcement information.

Technical source data

View raw source data -- the machine-readable record this page's information was built from.

Retrieved by Public Health Trace:

Frequently asked questions

What does a Class III mean?

A situation in which use of or exposure to a product is not likely to cause adverse health consequences.

Is this recall still active?

According to FDA, this recall's status is "Terminated." Always confirm the current status using the source links below, since status can change after Public Health Trace last retrieved this record.

What should I do if I have this product?

Follow the instructions published by the responsible agency (see the source links below) -- recall guidance (e.g. dispose of the product, return it for a refund, or check for a specific lot number) varies by recall and is set by that agency, not by Public Health Trace.

Where can I find more official information?

The source links below, published by FDA, are the authoritative record for this recall, including any updates issued after this summary was retrieved.

This summary is based on the official source record referenced above. Public Health Trace does not state that any company or product is unsafe beyond what the official source has published. Read the full medical disclaimer.