Food recall: DG Baby Gripe Water herbal supplement with organic ginger and fennel extracts, 4 FL OZ (120 mL) Liquid Dietary…
Class I FDA enforcement event 82182. Recall start date: . Status in the FDA record: Terminated. Termination date: .
Reason for recall, in the words of FDA
Presence of an undissolved ingredient, citrus flavonoid.
Class I, in the words of FDA
a situation in which there is a reasonable probability that the use of or exposure to a violative product will cause serious adverse health consequences or death
Kingston Pharma LLC started this food recall on 7 Feb 2019. The firm address in the FDA record is in Massena, NY. FDA put the recall in Class I. FDA event 82182 has 1 product record. The first FDA enforcement report date is 13 Mar 2019. The record gives the status Terminated, with the termination date 17 Jul 2019.
It is important to note that most of the time recall classifications are determined after the recalling firm provides all of the information needed to determine the risk posed to public health. The classification and posting in the FDA Enforcement Report should not be seen as an expansion or change to a firm’s voluntary public warning.
FDA publishes these words. Source: FDA, Enforcement Reports, Important Note, read on . openFDA export of .
Distribution
In the words of FDA.
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
Recalling firm
Kingston Pharma LLC, Massena, NY.
Recalling firm: The firm that the FDA record names for a recall.
FDA records how the recall started: Voluntary: Firm initiated.
Products
1 product record in the event.
| Recall number | Product | Quantity | Class | Status | Report date |
|---|---|---|---|---|---|
| F-1171-2019 | 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 | 138,752 bottles | Class I | Terminated | 13 Mar 2019 |
openFDA, about the status: FDA does not update the status of a recall after the recall has been classified according to its level of hazard. As such, the status of a recall (open, completed, or terminated) will remain unchanged after published in the Enforcement Reports.
Source: openFDA, Drug Recall Enforcement Reports, Disclaimer.
Enforcement report: The FDA publication that lists recalls. It has one record for each product of a recall.
Enforcement event: All the product records that have one FDA event number. This site shows one event on one page.
Class I: The highest of the three FDA recall classes.
The event in context
- Food events that started in 2019
- 516
- Share of these events in Class I
- 35%
- Product records in this event
- 1Median of the firm: 1
- Events of the firm on the register
- 3
Other events of the firm
| Initiated | Product (first record) | Type | Class | Records |
|---|---|---|---|---|
| 20 Mar 2019 | DG health NATURALS For Infants 2+ Months+ baby Cough Syrup + Mucus, Natural Grape Flavor, 2 FL OZ (59 mL), UPC: 8 54954 | Food | Class II | 1 |
| 29 Jan 2018 | Live Better Drug Free Black Elderberry Syrup, 4 FL OZ (118 mL); DIETARY SUPPLEMENT, UPC 050428581186 | Food | Class II | 1 |
Official channels
- FDA enforcement report F-1171-2019The FDA record of the first product of this event.
- FDA: recalls, market withdrawals and safety alertsThe recall notices on the FDA site.
- FDA: report a problemThe FDA page that shows where a report about a product goes.
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Cite this page
Recall Register. FDA enforcement event 82182. https://recallregister.com/fda/i/82182/. Source: openFDA enforcement reports. Data through .
Sources
- Source
- openFDA food enforcement reports
- Licence
- CC0 1.0
- Export date
- 28 Sep 2026
- Newest FDA report date on the register
- 23 Sep 2026
FDA has one record for each product. This site puts the records with the same event number on one page. The class of the event is the highest class of its records. How the register is made. Report an error.
Questions
- Where was the product distributed?
- The FDA record gives this 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
- What quantity of product is in FDA event 82182?
- The FDA record gives this quantity:
138,752 bottles
- How did the recall start?
- The FDA record says:
Voluntary: Firm initiated
- How many food recalls of 2019 have the same class?
- 35% of the 516 food events that started in 2019 are in Class I.