FDA recall record

M.O.M Enterprises, LLC Organic BABY bedtime drops recall — FDA H-0025-2026

Potential yeast contamination.

Class IIclassification
H-0025-2026official record ID
Oct 15, 2025report date

Recall record at a glance

Official recordH-0025-2026
CategoryFood Recalls
ClassificationClass II
FDA record statusOngoing
Recalling firmM.O.M Enterprises, LLC.
Report dateOct 15, 2025
Recall initiation dateSep 12, 2025
Quantity46,752 units/bottles (Lot 25100: 8,424 units; Lot 25148: 16,488 units; Lot 25155: 21,840 units)
LocationRichmond, CA, United States

Official product description

Organic BABY bedtime drops; sleep + immunity blend; Promotes restful sleep with natural herbs & supports immunity with elderberry & vitamin C; LIQUID DIETARY SUPPLEMENT; AGE 4 MONTHS+, NET WT. 2 OZ (60 ML)

Why the product was recalled

Potential yeast contamination.

Distribution information

AL, AR, AZ, CA, CO, CT, DE, FL, GA, IA, IL, IN, KS, KY, LA, MI, MN, MO, MS, NC, ND, NH, NJ, NY, OH, OR, PA, SC, TN, TX, UT, VA, WI

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Letter.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

Recall Lookup USA preserves the most complete source information successfully retrieved. We do not create missing facts or infer affected lots or VINs. The official record may still change, so use the identifier above when verifying current instructions.

FDA source limitation: openFDA enforcement reports are a reference dataset, not a live public-alert or recall-lifecycle service. FDA notes that enforcement-report status may not be updated after classification. Confirm current actions with the FDA, recalling firm or appropriate healthcare professional when relevant.

Related recall records

Other records from the same recalling company are shown first when available.