CLASS II ONGOING Food recall · Reported 23 Jul 2025 · FDA Enforcement Report

Little Remedies¿ Honey Cough recalled by Prestige Brands Holdings

Prestige Brands Holdings is recalling Little Remedies¿ Honey Cough, distributed nationwide in the US. The recall was initiated on 18 Jun 2025 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesUPC:7-56184-10737-9 Lot: 0039 Expiration: 11/2025 Lot: 0545 Expiration: 01/2026 Lot: 0640 Expiration: 02/2026 Lot: 0450 Expiration: 05/2026 Lot: 1198 Expiration: 12/2026
Quantity recalled10,223 cases (245,352 units)

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

Recall details

Recall number
H-0260-2025
FDA event ID
97088
Recalling firm
Prestige Brands Holdings, Tarrytown, NY
Classification
Class II
Status
Ongoing
Recall initiated
18 Jun 2025
FDA classified
11 Jul 2025
Reported
23 Jul 2025
Type
Voluntary: Firm initiated
Customers notified by
Press Release
Product category
Honey & Syrup

Timeline

18 Jun 2025Recall initiated by company
11 Jul 2025Classified by FDA+23 days
23 Jul 2025Published in enforcement report+12 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

contaminated with Bacillus cereus and may be spoiled

Product as listed by the FDA

Little Remedies¿ Honey Cough 4 FL OZ (118 mL)

Where it was distributed

Nationwide

Nationwide

Questions about this recall

Why was it recalled?

contaminated with Bacillus cereus and may be spoiled

Which lots are affected?

UPC:7-56184-10737-9 Lot: 0039 Expiration: 11/2025 Lot: 0545 Expiration: 01/2026 Lot: 0640 Expiration: 02/2026 Lot: 0450 Expiration: 05/2026 Lot: 1198 Expiration: 12/2026

Where was it sold?

Nationwide

What should I do if I have it?

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

What does Class II mean?

Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.

Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

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