LSL Healthcare Inc.: Device Recall
Recall #Z-1219-2026 · 12/22/2025
Class II: Risk
Recall Details
- Recall Number
- Z-1219-2026
- Classification
- Class II
- Product Type
- Device
- Recalling Firm
- LSL Healthcare Inc.
- Status
- Ongoing
- Date Initiated
- 12/22/2025
- Location
- Niles, IL, United States
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 1400 kits
Reason for Recall
BD ChloraPrep Triple Swabsticks, a component within the kits, exhibit an open seal on the packaging of the applicators.
Product Description
LSL Healthcare, Central Line Dressing Kit, Model/Catalog Number: 2519CP, medical procedure convenience kit
Distribution Pattern
US Nationwide distribution in the state of Idaho.
Data from FDA openFDA enforcement reports. This site is not affiliated with or endorsed by the FDA. Recall information may be updated by the FDA at any time.