ACTIVE RECALL — CLASS IIActive recallH-0025-2026/FDA enforcement

Organic Baby Bedtime Drops

What you need to know

Class II
  • What happened

    Potential yeast contamination.

  • Health risk

    The product may cause temporary or medically reversible health consequences, or the probability of serious harm is remote. A safety issue that does not fit the standard pathogen, allergen, chemical or quality categories.

  • Action required

    Stop taking the supplement. Check the lot and UPC codes below, then return it to the retailer or contact the manufacturer about a refund. Seek medical advice if you have concerns about exposure.

Active recall · classified by the FDAAL, AR, AZ, CA +29 moreMore supplements

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Product identification

Source: FDA FOOD

Brand nameM.o.m Enterprises, LLC.
Recalling firmM.o.m Enterprises, LLC.Richmond, CA, United States
UPC / barcodes
6 79234 05181 4
Lot / date codes
  • Lot code: 25100, 25148, 25155 UPC: 679234051814 EXP 04/2027, 05/2027, 06/2027
Distribution area
ALARAZCACOCTDEFLGAIAILINKSKYLAMIMNMOMSNCNDNHNJNYOHORPASCTNTXUTVAWI

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

United States

Quantity affected46, 752 units/bottles (Lot 25100: 8, 424 units; Lot 25148: 16, 488 units; Lot 25155: 21, 840 units)
Recall initiationFDA report date: October 15, 2025
FDA recall numberH-0025-2026

Beyond the headline

The recall, in context

M.o.m Enterprises, LLC. initiated this supplements recall on September 12, 2025. The FDA enforcement report states: Potential yeast contamination. The FDA report lists distribution as: 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.

The FDA enforcement report describes the reason as: Potential yeast contamination.

Organic Baby Bedtime Drops was made or distributed by M.o.m Enterprises, LLC. in Richmond, CA, United States. This page reflects FDA report H-0025-2026, dated October 15, 2025.

Why this is a Class II recall

Class II means the product may cause temporary or medically reversible health consequences, or the probability of serious harm is remote. In this recall, a safety issue that does not fit the standard pathogen, allergen, chemical or quality categories.

FDA definition

The product may cause temporary or medically reversible health consequences, or the probability of serious harm is remote.

What to do now

  1. 1

    Stop using it

    Do not eat, drink or take the affected product.

  2. 2

    Check the codes

    Compare the UPC and lot code against the table above.

  3. 3

    Return or discard

    Contact the retailer or recalling firm about a refund, and dispose of the product safely.

Consumer safety guide

Product safety recall

Symptoms to watch for

The official enforcement report describes the specific risk. Follow the recall notice, check the product codes and do not use a product that may be affected.

Higher-risk groups

Children, pregnant people, older adults and people with weakened immune systems should take extra care when a product's safety is uncertain.

What to do now

  1. 1Stop using or eating the product and keep it away from children and pets.
  2. 2Check the UPC and lot/date codes on this page and follow the official recall notice for disposal or return.
  3. 3Seek medical advice if anyone develops severe or worrying symptoms after exposure.

Read the official source record for the specific hazard and instructions.

This is general consumer safety information, not medical advice or a diagnosis. Follow the official recall notice and contact a healthcare professional if you have concerns about exposure or symptoms.

Frequently asked

Questions about this recall

What is the Organic Baby Bedtime Drops recall?

M.o.m Enterprises, LLC. recalled Organic Baby Bedtime Drops in an FDA Class II enforcement action reported as H-0025-2026. Potential yeast contamination.

What are the symptoms of Product safety recall exposure?

The official enforcement report describes the specific risk. Follow the recall notice, check the product codes and do not use a product that may be affected.

Who is most at risk from Product safety recall?

Children, pregnant people, older adults and people with weakened immune systems should take extra care when a product's safety is uncertain.

What should I do if I bought this product?

Stop taking the supplement. Check the lot and UPC codes below, then return it to the retailer or contact the manufacturer about a refund. Seek medical advice if you have concerns about exposure. Stop using or eating the product and keep it away from children and pets. Check the UPC and lot/date codes on this page and follow the official recall notice for disposal or return. Seek medical advice if anyone develops severe or worrying symptoms after exposure.

How do I get a refund from M.o.m Enterprises, LLC.?

Contact the recalling company or the retailer where you purchased the product, quote the FDA recall number and ask about a refund or replacement. Keep the packaging, lot code and proof of purchase where possible. The FDA does not issue consumer refunds. Reference FDA recall H-0025-2026 and keep the packaging, lot code and proof of purchase if you have them.

Is the M.o.m Enterprises, LLC. recall still active?

Yes. As of the latest FDA enforcement report, this recall is listed as ongoing. Check the official source record for the most current status before making a decision.

Where can I verify this recall?

This page is normalized from the openFDA enforcement record H-0025-2026. You can verify it directly using the official source link on this page. VerifyRecall updates its index from public FDA enforcement data and does not replace advice from the FDA, the recalling firm or a healthcare professional.

Verify before you act.

VerifyRecall is independent and not affiliated with the FDA. Always confirm the latest status on the official source record.

Official source

Brand history

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Record last synced from official openFDA enforcement data on November 14, 2026. Source record: official FDA notice.