Cardinal Health has issued a voluntary nationwide recall of select lots of Webcol Large Alcohol Prep Pads (70% isopropyl alcohol) after identifying microbial contamination with a bacterium called Paenibacillus phoenicis. The recall was announced March 19, 2026, and covers products distributed in the U.S., Puerto Rico, and Japan between September 2025 and February 2026. Cardinal Health warns there is a reasonable probability that use of the contaminated pads may result in local or systemic infections, with potentially life-threatening consequences for immunocompromised patients.
What’s Being Recalled?
The recalled product is Webcol Large Alcohol Prep Pads, 70% isopropyl alcohol, sold in boxes of 200 individually wrapped 2-ply pads. The pads are typically used for skin cleansing before injections, blood draws, and wound care. The recall covers select lot numbers distributed between September 2025 and February 2026. A full list of affected lot numbers is available via the FDA recall page and on a downloadable table from Cardinal Health. The lot number and product code can be found on both the inner carton label and the outer case label.
Why Was This Product Recalled?
Testing found the affected pads contaminated with Paenibacillus phoenicis, a bacterium that can cause serious infection when introduced into the body during skin preparation procedures. Although alcohol prep pads are for external use only, they are applied directly before needle insertion or skin breaks — meaning contaminated pads could introduce bacteria into the bloodstream or tissue. Cardinal Health states there is a reasonable probability the contamination could cause local infections, bacteremia (bloodstream infection), or central nervous system infections. The risk is highest for immunocompromised individuals — including patients with cancer undergoing chemotherapy or those with poorly controlled diabetes. No confirmed illnesses have been reported as of the recall announcement.
What Should You Do?
Stop using any Webcol Large Alcohol Prep Pads from affected lots immediately. Check the lot number on the inner carton or outer case label against the full list on the FDA’s website at fda.gov. Healthcare providers should segregate and quarantine affected product following Cardinal Health‘s return instructions. Consumers with questions can contact Cardinal Health at 800-292-9332, Monday through Friday, 8 a.m. to 5 p.m. EST, or email [email protected]. If you believe you’ve experienced a reaction after using these pads, contact your healthcare provider and report the event to FDA MedWatch at fda.gov/safety/medwatch.
