Kramer Laboratories is recalling about 14,250 units of Safetussin Max Strength Multi-Symptom Cough, Cold and Flu (acetaminophen, dextromethorphan HBr, and guaifenesin) 24-count caplet blister packs. The packaging of these products is not child-resistant as required by federal law because the tablets can be easily pushed through the foil. Consumers should immediately move the medicine to a location that is out of reach of children and contact the manufacturer for a full refund.
The foil packaging allows children to easily access the medication, posing a serious risk of poisoning if the caplets are accidentally swallowed. No injuries or incidents have been reported to date.
Consumers should immediately secure the product out of the sight and reach of children and contact Kramer Laboratories for information on how to return or dispose of the product for a full refund. Only the packaging is being recalled, not the medicine itself, but both should be disposed.
Product is sold in a blue, orange, and red cardboard box with a drug facts label on the back; labeled 'Safe for adults with High Blood Pressure, Diabetes'.
Recalled Safetussin Max Strength Multi-Symptom Cough, Cold and Flu, 24-count caplets
If you or a family member were harmed by this recalled product, you may have legal rights. Consider consulting a consumer protection attorney to understand your options for compensation.
This is general information, not legal advice. Go Backs is not a law firm and does not provide legal services.
AI-Enhanced Content: The summary, action steps, and risk assessment on this page were generated by AI from official government recall data to improve readability. This is not legal or medical advice. Always refer to the official agency sources below for authoritative information.
Sources: CPSC Notice · Raw API Response