FDA Medical devices recall ·
LSL Healthcare, Central Line Dressing Kit, Model recall
- Recall number
- Z-1219-2026
- Date
- (initiated December 22, 2025)
- Company / brand
- LSL Healthcare Inc.
6200 W Howard St, Niles, IL, United States - Category
- Medical devices › Class II
- Classification
- Class II
- Status
- Ongoing
- Units affected
- 1400 kits
- Initiated by
- Voluntary: Firm initiated
Read the official FDA notice ↗
Product
LSL Healthcare, Central Line Dressing Kit, Model/Catalog Number: 2519CP, medical procedure convenience kit
Why was it recalled?
BD ChloraPrep Triple Swabsticks, a component within the kits, exhibit an open seal on the packaging of the applicators.
What should you do?
FDA enforcement reports do not list a consumer remedy. Check the product codes below against what you have; if it matches, stop using it and follow the instructions in the firm's or FDA's official notice, or contact the company. If you have health concerns, contact your healthcare provider.
Product codes & lot numbers
Lot Code: Model No. 2519CP; UDI-DI 00661392048157; Lot# 5G3119; Expiration Date 7/31/26 GTIN: (01)00661392048157(10)5G3119(17)260731
Distribution
US Nationwide distribution in the state of Idaho.
States: Idaho
What does Class II mean?
Class II means use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or the probability of serious harm is remote.
Source: FDA (medical devices), recall Z-1219-2026. Official notice. Republished from public data; RecallFlag is not affiliated with the FDA.