CLASS I Food recall · Reported 13 Mar 2019 · FDA Enforcement Report
DG Baby Gripe Water herbal supplement recalled by Kingston Pharma
Kingston Pharma is recalling DG Baby Gripe Water herbal supplement with organic ginger and fennel extracts Liquid, distributed in 43 states. The recall was initiated on 7 Feb 2019 and the FDA has classified it as Class I.
Check your package
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-1171-2019
- FDA event ID
- 82182
- Recalling firm
- Kingston Pharma, Massena, NY
- Classification
- Class I
- Status
- Terminated
- Recall initiated
- 7 Feb 2019
- FDA classified
- 15 Mar 2019
- Reported
- 13 Mar 2019
- Type
- Voluntary: Firm initiated
- Customers notified by
- Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
- Reason category
- Other Reasons
- Product category
- Herbal Supplements
Timeline
| 7 Feb 2019 | Recall initiated by company | |
| 13 Mar 2019 | Published in enforcement report | +34 days |
| 15 Mar 2019 | Classified by FDA | +2 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
Presence of an undissolved ingredient, citrus flavonoid.
Product as listed by the FDA
DG Baby Gripe Water herbal supplement with organic ginger and fennel extracts, 4 FL OZ (120 mL) Liquid Dietary Supplement UPC: 8 54954 00246 3
Where it was distributed
USA: OH, FL, AZ, WI, MI, AL, CO, UT, NY, OK, CA, MO, IL, PA, CT, GA, TX, TN, NE, MA, OR, VA, NJ, IA, IN, KY, OK, LA, AR, KS, SC, MS, WV, NC, MD, DE, ME, MN, ND, NH, NV, RI, SD, VT
AlabamaArkansasArizonaCaliforniaColoradoConnecticutDelawareFloridaGeorgiaIowaIllinoisIndianaKansasKentuckyLouisianaMassachusettsMarylandMaineMichiganMinnesota
Questions about this recall
Why was it recalled?
Presence of an undissolved ingredient, citrus flavonoid.
Which lots are affected?
All lot codes.
Where was it sold?
USA: OH, FL, AZ, WI, MI, AL, CO, UT, NY, OK, CA, MO, IL, PA, CT, GA, TX, TN, NE, MA, OR, VA, NJ, IA, IN, KY, OK, LA, AR, KS, SC, MS, WV, NC, MD, DE, ME, MN, ND, NH, NV, RI, SD, VT
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 I mean?
Class I is the most serious FDA recall category: there is a reasonable probability that using the product will cause serious health consequences or death.
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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