Medtech recalls Little Remedies® honey cough syrup
On June 17, 2025, Medtech Products Inc., a subsidiary of Prestige Consumer Healthcare Inc., announced a voluntary recall of five lots of its Little Remedies® Honey Cough Syrup. This action has been taken due to the detection of Bacillus cereus and concerns regarding the product’s shelf stability. Bacillus cereus is a bacterium that can cause foodborne illnesses, potentially posing health risks, particularly to young children.
Reason for recall
The recall was initiated after testing revealed that the affected lots of Little Remedies® Honey Cough Syrup contained Bacillus cereus. The presence of this bacterium can lead to food poisoning, resulting in symptoms that may include nausea, vomiting, and diarrhea. Additionally, the loss of shelf stability compromises the product’s effectiveness and safety.
Health risks associated with Bacillus cereus
Bacillus cereus is a well-known pathogen, especially in food products, known to cause gastrointestinal illness. While healthy individuals may recover without medical intervention, the bacteria can be more dangerous for vulnerable populations such as infants and young children. Therefore, it’s crucial for parents to be aware of the potential health risks associated with medicinal products containing this bacterium.
Recommended actions for consumers
Consumers who possess the recalled Little Remedies® Honey Cough Syrup are advised to stop using the product immediately. They should check their homes for any of the affected lots, which can be identified on the packaging. For a full list of the impacted lot numbers and details on how to obtain a refund, consumers are encouraged to visit the company’s website or contact their customer service.
Importance of product recalls
Product recalls serve a vital role in ensuring public safety. They are initiated to protect consumers from products that may pose health risks or safety issues. The swift action taken by Medtech reflects a commitment to consumer health and safety, highlighting the importance of adherence to safety regulations and quality control in the healthcare industry.
Reporting adverse effects to the FDA
Consumers who experience any adverse health effects or reactions after using the recalled product are urged to report these incidents to the FDA. Feedback is essential for monitoring public health and ensuring the safety of all products on the market. The FDA provides a user-friendly platform for submitting adverse event reports through its MedWatch program.
For more information on the recall and to check for specific lot numbers, please visit the official FDA announcement here.
Source : www.fda.gov
