FDA recall, , Moderate risk
LSL Healthcare Central Line Dressing, Foley Urine Collection, IV Start and Wound Closure Kits
Medical procedure kits contain alcohol prep pads that may not be sterile.
Summary by Recall Canary from the FDA notice
What happened
LSL Healthcare Inc., of Niles, Illinois, recalled medical procedure kits because they were distributed containing Webcol Large Alcohol Prep Pads which were subsequently recalled for non-sterility. The recall began March 9, 2026, and was added to the FDA's Enforcement Report on April 22, 2026. The products were distributed nationwide in the states of Maryland, Illinois, and Minnesota.
What to do
We don't have product-specific instructions for this recall. FDA's general advice for medical device recalls:
- A device recall doesn't always mean you must stop using it: it may need to be checked, adjusted or fixed.
- Talk to your health care provider before you stop using it.
Is your kit affected?
6 products
Match the UDI-DI, lot code and catalog code listed under your product.
A UDI-DI is the device identifier printed with the barcode on the device label.
LSL Healthcare, Standard Central Line Dressing Change Kit, Model/
- UDI-DI
- 00661392054721
- Catalog code
- 2717J
- Lot code
- 6A3043
- 6B3076
LSL Healthcare Wound Closure Tray, Model/
- UDI-DI
- 00661392008342
- Catalog code
- 7554
- Lot code
- 6A3146
LSL Healthcare, Foley Urine Collection Kit, Model/
- UDI-DI
- 00661392002326
- Catalog code
- 1555
- Lot code
- 260221
LSL Healthcare, IV Start Kit, Model/
- UDI-DI
- 00661392054271
- Catalog code
- 3131
- Lot code
- 6A3139
LSL Healthcare, Central Line Dressing Kit, Model/
- UDI-DI
- 00661392054738
- Catalog code
- 2717H
- Lot code
- 6A3181
LSL Healthcare, Infant Central Line Dressing Change Kit, Model/
- UDI-DI
- 00661392052635
- Catalog code
- 2925H
- Lot code
- 6B3022
Recall details
- Company began the recall
- Company
- LSL Healthcare Inc.Niles, Illinois
- Hazard
- Sterility problem
- Risk
Moderate risk
Using it may cause short-term health problems, or ones that treatment can reverse. Serious harm is unlikely.
FDA Class II recall · How risk is rated
- Event ID
- 98631
- Recall numbers
- Z-1928-2026 to Z-1933-2026
- Recall type
- Voluntary: Firm initiated
- How the company first told customers
All recalls from LSL Healthcare Inc.
Timeline
FDA's Enforcement Report is its public list of recalls; FDA adds a recall when it posts it and publishes the list weekly.
Company began the recall
Added to FDA's Enforcement Report · Classified by FDA
Listed on Recall Canary
In FDA's weekly enforcement report
Summary updated
