CLASS III Food recall · Reported 29 Mar 2023 · FDA Enforcement Report

DG Health Sugar Free Daily Fiber recalled by Dollar General

Dollar General is recalling DG Health Sugar Free Daily Fiber (, distributed in 47 states. The recall was initiated on 1 Mar 2023 and the FDA has classified it as Class III.

Check your package

Lot, batch or date codesBatch 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 recalled89,136 units

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

Recall details

Recall number
F-0650-2023
FDA event ID
91809
Recalling firm
Dollar General, Goodlettsville, TN
Classification
Class III
Status
Terminated
Recall initiated
1 Mar 2023
FDA classified
23 Mar 2023
Reported
29 Mar 2023
Type
Voluntary: Firm initiated
Customers notified by
E-Mail
Reason category
Foreign Material
Product category
Other

Timeline

1 Mar 2023Recall initiated by company
23 Mar 2023Classified by FDA+22 days
29 Mar 2023Published in enforcement report+6 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

Product is missing warning declaration that it contains phenylalanine.

Foreign material recalls cover pieces of metal, plastic, glass, wood or other objects that got into the product during processing and could cause injury if eaten.

Product as listed by the FDA

DG Health brand Sugar Free Daily Fiber in 10 oz. plastic containers (UPC: 860005934294).

Where it was distributed

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.

AlabamaArkansasArizonaCaliforniaColoradoConnecticutDelawareFloridaGeorgiaIowaIdahoIllinoisIndianaKansasKentuckyLouisianaMassachusettsMarylandMaineMichigan

Stores named: Dollar General

Questions about this recall

Why was it recalled?

Product is missing warning declaration that it contains phenylalanine.

Which lots are affected?

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

Where was it sold?

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.

What should I do if I have it?

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

What does Class III mean?

Class III recalls are for products unlikely to cause any adverse health consequence, usually labelling or quality issues.

Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

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