RecallHawk
Class II Recall

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

Prestige Brands Holdings

Summary

The FDA issued a Class II for Little Remedies¿ Honey Cough 4 FL OZ (118 mL) by Prestige Brands Holdings. Reason: contaminated with Bacillus cereus and may be spoiled.

Details

Source

Food Recall

External ID

H-0260-2025

Action Date

2025-07-23

Status

Ongoing

Category

food

Product Description

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

Lot/Code Info: 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

Quantity Affected: 10,223 cases (245,352 units)

Reason for Recall

contaminated with Bacillus cereus and may be spoiled

Distribution

Nationwide

Type: Voluntary: Firm initiated

Recall Initiated: 2025-06-18

Company

Context & Analysis

This is a Class II recall. Class II recalls indicate that use of or exposure to the product may cause temporary or medically reversible health consequences, or that the probability of serious consequences is remote.

This was one of 98 food recalls issued in the same week, part of 204 food-related FDA actions this month.

Frequently Asked Questions

What is a Class II recall?

A Class II recall means the product may cause temporary or medically reversible adverse health consequences, or the probability of serious adverse consequences is remote. Consumers should discontinue use.

What should I do if I have this product?

Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (Prestige Brands Holdings) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does Prestige Brands Holdings have FDA actions?

This is the only FDA action we have on record for Prestige Brands Holdings in our database.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "H-0260-2025" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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