Food Recall Check
Class I · High risk Terminated Initiated Feb 7, 2019 (8 years ago)

DG Baby Gripe Water herbal supplement with organic ginger and fennel extracts recall

Recalled by Kingston Pharma LLC · Massena, NY, United States

Class I — High risk. Reasonable probability of serious harm or death.

Why it was recalled

Presence of an undissolved ingredient, citrus flavonoid.

See the recall's own reason text for the specifics. All other reasons recalls.

What 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

Quantity: 138,752 bottles

Food: Dietary supplements Juice & beverages

Lot codes, dates and UPCs

A recall covers only these codes. Compare them with the lot number, best-by date or UPC printed on your package.

All lot codes.

Where it was sold

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

FDA's distribution note: 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

Do not eat it. Class I means FDA judged there is a reasonable probability of serious illness or death. If the brand, size and lot or date code on your package match, throw the product away or return it to the store for a refund, and clean any surface or container it touched. If anyone has eaten it and feels unwell, contact a doctor and mention the recall. FDA lists this recall as terminated: the company has finished removing the product, so it should no longer be on shelves - but it can still be in a freezer or pantry.

Recalling firm
Kingston Pharma LLC
Initiated by
Voluntary: Firm initiated
Recall initiated
Feb 7, 2019
In FDA report of
Mar 13, 2019
Terminated
Jul 17, 2019
FDA recall number
F-1171-2019 · event 82182
Official record
FDA enforcement report search

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