CareFusion 213, LLC — FDA Class I (D-0625-2026)

CareFusion 213, LLC is recalling 178,000 applicators of a chlorhexidine topical product due to non-sterility. The recall is due to contamination issues. This action is taken to protect consumer safety.

• •CareFusion 213, LLC is recalling 178,000 chlorhexidine applicators.
• •The recall is due to contamination, making the product non-sterile.
• •This is a Class I recall due to serious health risks.
• •Consumers should check their medicine cabinets for the recalled product.

Consumers using the recalled 178,000 applicators should stop using them immediately to avoid health risks from contamination.