LSL Healthcare — Class II medical device recall Z-1219-2026
Ongoing recall by LSL Healthcare Inc., reported 2026-02-04, distributed nationwide. BD ChloraPrep Triple Swabsticks, a component within the kits, exhibit an open seal on the packaging of the app
| Recall number | Z-1219-2026 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | LSL Healthcare Inc., Niles, IL, United States |
| Recall initiated | 2025-12-22 |
| Classified | 2026-01-29 |
| Reported by FDA | 2026-02-04 |
| Distributed | Nationwide (US) |
| Quantity | 1,400 kits |
| Reason classes | packaging |
| UPC / GTIN / UDI-DI | 00661392048157 |
| Lot numbers | 5G3119 |
| Model numbers | 2519CP |
| Expiration dates | 2026-07-31 |
Product
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.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-1219-2026. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.