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Prestige Brands Holdings Recall: contaminated with Bacillus cereus and may be spoiled

United States

OngoingClass II

Company
Prestige Brands Holdings
Product
Little Remedies¿ Honey Cough 4 FL OZ (118 mL)
Recall date
June 18, 2025
Source
FDA

Reason for recall

contaminated with Bacillus cereus and may be spoiled

  1. - Recall initiated
  2. - Reported by source
Recalled products
Product description UPC Quantity Lot / code information
Little Remedies¿ Honey Cough 4 FL OZ (118 mL) Not published in this source record 10,223 cases (245,352 units) 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

Distribution

  • Nationwide

Official source record

Agency
FDA
Dataset
FDA Food Enforcement (Recalls)
Recall number
H-0260-2025
Event ID
97088
Status
Ongoing
Classification
Class II
Company
Prestige Brands Holdings
Product description
Little Remedies¿ Honey Cough 4 FL OZ (118 mL)
Quantity
10,223 cases (245,352 units)
Reason
contaminated with Bacillus cereus and may be spoiled
Recall initiation date
June 18, 2025
Report date
July 23, 2025
Classification date
Not published in this source record
Termination date
Not terminated as of this source record
Distribution pattern
Nationwide
UPC, lot, and code information
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
Voluntary or mandated
Voluntary: Firm initiated
Initial notification method
Press Release
Source last updated
Not tracked separately from the Public Health Trace retrieval date below
Public Health Trace retrieval date

Responsible company: Prestige Brands Holdings

Other recalls from Prestige Brands Holdings

FDA Recall Ongoing 2026 recordClass II

CLEAR EYES Maximum Itchy Eye Relief, 0.5 fl oz (15 mL) per dropper bottle, Sterile, Dist. by Medtech Products Inc., Tarrytown, NY 10591, a Prestige Consumer Healthcare Company. NDC: 67172-999-01 UPC 6 78112 65920 3

by Prestige Brands Holdings

Published
August 19, 2026
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass III

PediaCare brand DAY & NIGHT Value Pack DAYTIME MULTI-SYMPTOM Cold (dextromethorphan HBr 5 mg and Phenylephrine HCl 2.5 mg) and NIGHTTIME MULTI-SYMPTOM Cold (diphenhydramine HCl 6.25 mg and phenylephrine HCl 2.5 mg), 4 FL oz (118 mL) bottles, one each of DAYTIME MULTI-SYMPTOM Cold, Distributed by Medtech Products, Inc., Tarrytown, NY --- UPC 814832013523

by Prestige Brands Holdings

Published
June 4, 2014
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass III

PediaCare brand NIGHTTIME MULTI-SYMPTOM Cold, (diphenhydramine HCl 6.25 mg and phenylephrine HCl 2.5 mg), 4 FL OZ (118 mL), Distributed by Medtech Products, Inc., Tarrytown,NY ---- UPC 814832013544

by Prestige Brands Holdings

Published
June 4, 2014
Distribution
Nationwide

View recall →

Where this information comes from

View FDA enforcement record -- the specific openFDA record this summary was built from.

No separate FDA public notice was found for this enforcement record. The information below comes from FDA's Recall Enterprise System through openFDA.

FDA Enforcement Reports -- FDA's general, official recall and enforcement information.

Technical source data

View raw source data -- the machine-readable record this page's information was built from.

Retrieved by Public Health Trace:

Frequently asked questions

What does a Class II mean?

A situation in which use of or exposure to a product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote.

Is this recall still active?

According to FDA, this recall's status is "Ongoing." Always confirm the current status using the source links below, since status can change after Public Health Trace last retrieved this record.

What should I do if I have this product?

Follow the instructions published by the responsible agency (see the source links below) -- recall guidance (e.g. dispose of the product, return it for a refund, or check for a specific lot number) varies by recall and is set by that agency, not by Public Health Trace.

Where can I find more official information?

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