LSL Healthcare, Standard Central Line Dressing Change Kit… recallZ-1929-2026 · LSL Healthcare Inc. · initiated Mar 9, 2026
Open, Classified
Is my device affected?
- Compare the model, catalog and lot or serial numbers on your device or its packaging with the code information below. A recall usually covers only specific models or lots.
- If yours is listed, follow the instructions from LSL Healthcare Inc. or your healthcare provider. The company's action is summarized under what the company is doing.
- Do not stop using a prescribed or implanted device on your own — talk to your healthcare provider first.
Where to find your model and lot numbers · What recall classes and statuses mean
Why it was recalled
Medical procedure kits were distributed containing Webcol Large Alcohol Prep Pads which were subsequently recalled for non-sterility.
FDA root cause category: Under Investigation by firm
What the company is doing
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].
Recall details
- Recall number
- Z-1929-2026
- Status
- Open, Classified
- Initiated by the company
- Mar 9, 2026
- Posted by the FDA
- Apr 22, 2026
- Recalling firm
- LSL Healthcare Inc.
- Quantity
- 3460 units
- Product code
- OXQ
- Distribution
- US Nationwide distribution in the states of MD, IL, MN.
Product description
LSL Healthcare, Standard Central Line Dressing Change Kit, Model/Catalog Number: 2717J
Code information (models, lots, serial numbers)
Lot Code: Model No. 2717J; UDI-DI 00661392054721; Lot# 6A3043, Expiration Date 11/30/2026. Lot#6B3076, Expiration Date 01/31/2027 GTIN: (01)00661392054721(10)6A3043(17)261130 GTIN: (01)00661392054721(10)6B3076(17)260131
Devices named in this recall
1 device in the FDA device registry whose identifier appears in the recall's code information.
- LSL HEALTHCARE 2717JLSL Industries, LLC · Dressing change tray1 recall0 reports
Other products in the same recall event
The FDA groups related products into one recall event (event 98631).
- Z-1928-2026 · Open, ClassifiedLSL Healthcare, Central Line Dressing Kit, Model/Catalog Number: 2717H
- Z-1930-2026 · Open, ClassifiedLSL Healthcare, Foley Urine Collection Kit, Model/Catalog Number: 1555
- Z-1931-2026 · Open, ClassifiedLSL Healthcare, Infant Central Line Dressing Change Kit, Model/Catalog Number: 2925H
- Z-1933-2026 · Open, ClassifiedLSL Healthcare Wound Closure Tray, Model/Catalog Number: 7554
Sources and updates
- Recall record: FDA Medical Device Recalls, file dated Oct 16, 2026 · View the FDA recall notice ↗
- Devices: FDA GUDID, file dated Oct 13, 2026. Devices are linked when their identifier (with a valid check digit) appears in the recall's code information.
- Page last rebuilt: Oct 16, 2026. Text above is shown as published by the FDA.
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