PlainRecalls
CriticalClass ITerminated

FDA Food recall · Reported March 13, 2019

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

Presence of an undissolved ingredient, citrus flavonoid.

Recall #
F-1171-2019
Affected scope
138,752 bottles
Initiated
February 7, 2019
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Kingston Pharma LLC recalled DG Baby Gripe Water herbal supplement with organic ginger and fennel extracts, 4 FL OZ (1… - a critical-severity action.

DG Baby Gripe Water herbal supplement with organic ginger and fennel extracts, 4 FL OZ (1… was recalled by Kingston Pharma LLC in March 13, 2019. Reason: Presence of an undissolved ingredient, citrus flavonoid.. Check the official notice for the remedy. Verify recall #F-1171-2019 with the FDA Food before acting.

The recall

Kingston Pharma LLC issued this critical-severity FDA Food recall-Presence of an undissolved ingredient, citrus flavonoid..

Critical
severity level
Class I
classification
March 13, 2019
reported

Sourced from official FDA Food enforcement records. Verify recall #F-1171-2019 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.

Recall Insight

This FDA Food action (record #F-1171-2019) was formally reported on March 13, 2019, with the manufacturer initiating the action on February 7, 2019. It is classified under Critical severity (Class I), with a current status of Terminated. Kingston Pharma LLC is listed as the recalling firm, operating out of Massena, NY. Federal records list the affected scope as 138,752 bottles.

The documented reason for this recall is: Presence of an undissolved ingredient, citrus flavonoid. Distribution data in the federal record shows the product reached: 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. Distribution scope directly affects the consumer exposure window and determines whether a recall remains regional or escalates into a nationwide advisory.

Within the same product category the archive holds 6 closely related recalls - clustering in a narrow category often points to a systemic quality-control or supplier issue rather than a one-off defect. Always verify the recall number against the official agency record before acting.

Children & Baby Products recalls over time

Where this recall sits in its category - 3,772 children & baby products recalls on record

0100200300400500600 20052008201120142017202020232026 187
Severity1902064468High severity (most serious)Moderate severityLow severity
Where this agency-classified recall sits among FDA Class I/II/III notices

Of 88,001 recalls with an agency hazard classification, 19,020 are high severity, 64,468 moderate, and 4,513 low. A further 16,157 CPSC/NHTSA recalls have no agency class and are excluded from this split. This recall is classified high severity.

Counts reflect market size and reporting activity, not inherent danger, we do not rank products by risk from raw recall volume.

Severity

Critical

Affected scope

138,752 bottles

Related Recalls

6

0 from same agency

Product description

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

Reason for recall

Presence of an undissolved ingredient, citrus flavonoid.

Recall Profile

Structured summary of the FDA Food recall record
Attribute Value
Agency U.S. Food and Drug Administration
Severity class Critical (Class I)
Status Terminated
Recall number F-1171-2019
Date reported March 13, 2019
Date initiated February 7, 2019
Recalling firm Kingston Pharma LLC
Firm location Massena, NY
Affected scope 138,752 bottles
Distribution 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

Profile values are sourced directly from the official FDA Food enforcement record. Source: U.S. Food and Drug Administration.

What to do with this recall

Match your product against the recall record, then act on the agency remedy.

  • Check the recall number (F-1171-2019) and product description against the item you own. Search the archive
  • Confirm the current status with FDA Food before acting, recall details can be updated.
  • This is a Class I (high-risk) recall, stop using the product immediately and follow the disposal or return instructions. What to do next

This page summarizes the official FDA Food record for research and awareness; it is not legal, medical, or safety advice. Verify with the issuing agency before acting.

Frequently Asked Questions

What product was recalled?
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. Recalled by Kingston Pharma LLC. Units affected: 138,752 bottles.
Why was this product recalled?
Presence of an undissolved ingredient, citrus flavonoid.
Which agency issued this recall?
This recall was issued by the FDA Food on March 13, 2019. Severity: Critical. Recall number: F-1171-2019.
Where was the recalled product distributed?
Distribution: 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.
How do I check if my product is affected by a recall?
Check the product description and recall number (F-1171-2019) against your product. Visit the official FDA Food website for the most current information. You can also use our Recall Checker tool to search by product name or brand.
What are the health risks of consuming a recalled food product?
Recalled food products may contain contaminants, undeclared allergens, or harmful bacteria such as Salmonella, Listeria, or E. coli. Consuming these products can cause foodborne illness ranging from mild gastrointestinal symptoms to serious conditions requiring hospitalization. If you have consumed a recalled food product and experience symptoms, contact your healthcare provider and report to the FDA via MedWatch.

Nationwide recalls with similar severity or category timing

Two federal-filing-derived peer sets for this notice, both outside the same recalling firm and filing state so the neighborhoods are not firm or geographic containment.

Nearby Recalls in This Category

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Every figure on PlainRecalls is rendered directly from official FDA, CPSC and NHTSA recall records, no number is typed in by an editor. This recall: FDA Food, reported March 13, 2019. Severity classes follow each agency's own taxonomy (FDA Class I/II/III; CPSC and NHTSA by hazard type), and related-recall context is computed across the full archive. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error. Data current as of August 2026.