FDA recall, , Moderate risk
LSL Healthcare Central Line Dressing Kit
The Central Line Dressing Kit contains BD ChloraPrep Triple Swabsticks with an open seal on the applicator packaging.
Summary by Recall Canary from the FDA notice
What happened
LSL Healthcare Inc. of Niles, Illinois, recalled its LSL Healthcare, Central Line Dressing Kit, a medical procedure convenience kit, because BD ChloraPrep Triple Swabsticks, a component within the kits, exhibit an open seal on the packaging of the applicators. The recall began on December 22, 2025, and was added to the FDA's Enforcement Report on January 29, 2026.
The kits were distributed in Idaho. The recall involved 1400 kits.
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?
Match the model number, UDI-DI and lot code listed under your product.
A UDI-DI is the device identifier printed with the barcode on the device label.
LSL Healthcare, Central Line Dressing Kit
- Model number
- /Catalog Number: 2519CP
- 2519CP
- UDI-DI
- 00661392048157
- Lot code
- 5G3119
Recall details
- Company began the recall
- Sold in
US Nationwide distribution in the state of Idaho.
- Company
- LSL Healthcare Inc.Niles, Illinois
- Hazard
- Device defect
- 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
- 98245
- Recall number
- Z-1219-2026
- Quantity recalled
- 1400 kits
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
In FDA's weekly enforcement report
Listed on Recall Canary
