Neutrogena Recalls Makeup Wipes Due to Bacterial Contamination

The Food and Drug Administration (FDA) issued a Class II risk level for a line of Neutrogena's makeup-removing facial wipes due to potential bacterial infection, according to a statement from the agency.

In a brief message, the FDA reported that an internal investigation by the manufacturer (Kenvue) revealed the product had tested positive for plurabacter gergioviae, prompting the agency to issue a Class II risk level for the product.

The recall applies to the Neutrogena Makeup Remover Ultra-Soft Cleansing Towelettes (50-count), which come in 25-pack wipes containing the plant-based compostable towelettes.

The FDA statement said that the specific affected product quantity comprised 1,312 cases. Recalled lots of the product have been initiated in Texas, South Carolina, Georgia, and Florida. The voluntary recall (Recall No. C-0001-2026) has been ongoing since September 19.

Source: FDA statement. Accessed October 28, 2025.