Haleon Recalled Certain Robitussin Syrup Lots
The manufacturer issued a recall for eight specific cough syrup lots due to potential microbial contamination.
Updated on Oct. 9, 2026 in Allergies
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On January 24, 2024, Haleon announced a voluntary recall of eight lots of Robitussin Honey CF Max Day Adult and Nighttime Adult products. These syrups, typically used for temporary relief of cold, flu, and allergy symptoms, were flagged due to microbial contamination.
Why it matters
Recalls regarding microbial contamination are critical safety measures to prevent potential infections in consumers using over-the-counter products. This recall ensures that impacted medications are removed from distribution to protect public health.
Haleon reported the recall of eight specific product lots following concerns over microbial contamination. There have been no confirmed reports of adverse health events associated with these products to date.
The players
Haleon
A global consumer healthcare company based in Warren, NJ, that manufactures various over-the-counter medications for pain, respiratory health, and allergies.
The details
The recall focuses on microbial contamination, which can occur during the manufacturing or packaging process and may pose risks to individuals, particularly those with compromised immune systems. Haleon is currently managing the removal of these specific lots from the marketplace by notifying distributors and customers directly with instructions for returns.
Timeline
January 24, 2024: Haleon announced the voluntary recall of the affected Robitussin products.
Health Landscape
This recall follows the standard safety oversight procedures established by the FDA's voluntary recall process for consumer health products. It highlights the role of manufacturers in monitoring product quality to maintain public safety standards.
If you have purchased Robitussin Honey CF Max, check your product packaging against the affected lot numbers provided by the manufacturer. If you believe you have experienced a reaction to a medication, it is worth discussing those symptoms with your doctor.
The takeaway
Consumers should immediately stop using any products identified in the recall and follow return instructions provided by the manufacturer. For specific questions regarding the recalled lots or the return process, contact Haleon consumer relations at 1-800-245-1040.
Further reading
For broader guidance on managing symptoms safely, visit our section on Allergies.
More information
To report a side effect or product quality issue, use the FDA adverse event reporting portal.
Source note: This article includes information reported by U.S. Food and Drug Administration.
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