LSL Healthcare Inc. recalls LSL Healthcare

BD ChloraPrep Triple Swabsticks, a component within the kits, exhibit an open seal on the packaging of the applicators.

LSL Healthcare, Central Line Dressing Kit, Model/Catalog Number: 2519CP, medical procedure convenience kit

LSL issued issued an URGENT: Kit Component Recall notice to its sole consignee on 12/22/2025 via email. The notice explained the issue and requested the following actions: "1. Immediately stop using the affected kits in your facility. 2. Inspect all inventory locations within your facility and destroy all affected kits according to your facility's disposal process. If destruction is not feasible immediately, the products should be quarantined until proper disposal can occur. If disposal is not possible, please request a Return Merchandise Authorization (RMA) to return these kits as indicated below. 3. This recall should be executed at the distributor, hospital, and user levels. Identify all customers within your distribution network who may have purchased the affected products listed in this notification. Provide a copy of the attached customer letter to all of these customers to inform them of the recall on behalf of BD & LSL. 4. Complete the attached Response Form and return it to the LSL contact provided on the form if you have any of the affected products in stock. This will help LSL acknowledge your receipt of this notification. Please indicate the quantity of affected products identified in your facility and confirm whether this inventory was destroyed or returned. 5. If you require assistance with this process, please contact your LSL representative or reach out to LSL using the contact information provided below. LSL Industries LLS, dba LSL Healthcare 6200 W. Howard Street Nile, IL, 60714 (888) 225-5575 | lslorderinquiries@lslhealthcare.com" LSL will provide credit for any destroyed products from the specific lot numbers mentioned above to customers who purchased the affected items directly from LSL. This will occur upon receipt of the completed Response Form.

• FDA enforcement recordOfficial FDA database entry for Z-1219-2026
• FDA device classification · OWLOfficial FDA classification for this device type
• CFR regulation · 21 CFR 880.5200The federal regulation governing this device
• FDA recall announcementSearch FDA.gov for the official press announcement
• Find LSL Healthcare Inc.Search for the manufacturer's official notice
• News coverageRecent reporting on this recall and manufacturer
• openFDA data recordThe raw JSON record this page is built from

Source: U.S. FDA openFDA device enforcement reports. This summary is informational and may lag or differ from the official record. Always verify against the FDA before acting.