Warning
LSL Healthcare Inc. Recalls LSL Healthcare
This is a Class II recall. This product may cause temporary health problems or pose a slight threat of a serious nature.
Source: FDA
WarningRecall #Z-1931-2026Medical Device
LSL Healthcare Inc. Recalls LSL Healthcare
LSL Healthcare Inc. · Class II — Moderate Risk
Product Description
LSL Healthcare, Infant Central Line Dressing Change Kit, Model/Catalog Number: 2925H
Reason for Recall
Medical procedure kits were distributed containing Webcol Large Alcohol Prep Pads which were subsequently recalled for non-sterility.
FDA Classification
Class II — Moderate Risk
A situation in which use of, or exposure to, a violative product may cause temporary or medically reversible adverse health consequences, or where the probability of serious adverse health consequences is remote.
Distribution
US Nationwide distribution in the states of MD, IL, MN.
Remedy
Consumers should stop using this product. Contact the recalling firm for further instructions regarding this product.
411 Press Analysis
The FDA classified this recall as Class II, indicating the medical device may cause temporary health problems or poses a slight threat of a serious nature. LSL Healthcare Inc. initiated the recall on March 9, 2026 affecting 220 units. Medical procedure kits were distributed containing Webcol Large Alcohol Prep Pads which were subsequently recalled for non-sterility. The product was distributed in MD, IL, MN. Consumers should check their purchases and discontinue use of any affected product. Contact LSL Healthcare Inc. for further instructions.
Sources: FDA openFDA Enforcement Database
This recall appears in: Medical Device Defects.