Recall Z-1219-2026— LSL Healthcare Inc.
Class II · Ongoing
Class II FDA medical device recall by LSL Healthcare Inc., initiated 2025-12-22. FDA's recall record names no specific 510(k) clearance for this event. Product: LSL Healthcare, Central Line Dressing Kit, Model/Catalog Number: 2519CP, medical procedure convenience kit. Reason: BD ChloraPrep Triple Swabsticks, a component within the kits, exhibit an open seal on the packaging of the applicators..
- Recalling firm
- LSL Healthcare Inc.
- Classification
- Class II
- Status
- Ongoing
- Initiated
- 2025-12-22
- Firm location
- Niles, IL, United States
Product description
LSL Healthcare, Central Line Dressing Kit, Model/Catalog Number: 2519CP, medical procedure convenience kit
Reason for recall
BD ChloraPrep Triple Swabsticks, a component within the kits, exhibit an open seal on the packaging of the applicators.
Data sourced from openFDA. This site is unofficial and independent of the FDA.