LSL Healthcare, Standard Central Line Dressing Change Kit, Model/Catalog Number: 2717J
FDA Recall Z-1929-2026 · Posted 2026-04-22
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Recalling FirmLSL Healthcare Inc.
Recall StatusOpen, Classified
Product CodeOXQ
Date Initiated2026-03-09
Product Quantity3460 units
Reason for Recall
Medical procedure kits were distributed containing Webcol Large Alcohol Prep Pads which were subsequently recalled for non-sterility.
Firm Action
LSL Healthcare issued an UREGNT: Kit Component Recall to its consignees on 3/9/2026 via email. The notice explained the issue and requested the following:
"1. Immediately stop using the affected kits in your facility.
2. Inspection all inventory locations within your facility and destroy all affected kits according to your facility's disposal process. If immediate destruction is not feasible, 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..
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.
4. Complete the attached Response Form and return to the LSL contact provided on the form if you have any of the affected product in stock."
For assistance with this process, please contact your LSL representative or LSL at LSL Healthcare, 6200 W. Howard Street, Nile, IL 60714, (888)225-5575, [email protected].
Root Cause
Under Investigation by firm
Distribution Pattern
US Nationwide distribution in the states of MD, IL, MN.
Official Source
View FDA Recall →Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.
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