A recent recall of SinuCleanse nasal wash by the U.S. Food and Drug Administration has been classified as a Class 1 recall due to microbial contamination, posing a high risk to consumers. The recall, initiated in February, remains ongoing.
Ascent Consumer Products Inc. voluntarily recalled one lot of SinuCleanse Soft Tip Squeeze Bottle Nasal Wash System, which is commonly used for cold and flu symptoms and allergies. This recall was prompted by the detection of Staphylococcus aureus bacteria in the product. While this bacteria is commonly found on the skin and in nasal passages without causing infection, it can be fatal when it does.
The affected lot, labeled with lot number 024122661A1 and a best-by date of December 31, 2027, was distributed nationwide in January 2025. If you have this product, the FDA advises against using it and recommends disposing of it immediately or returning it to the point of purchase.
The FDA warns that using the contaminated nasal wash could lead to serious health consequences, particularly for individuals with compromised nasal cavities. Potential risks include blood infections, endocarditis, bone and joint infections, splenic abscesses, meningitis, bacterial sinusitis, eye tissue infections, vision problems, cranial nerve damage, and more.
If you have used the recalled product and experience any adverse reactions, seek immediate medical attention.
